MAXX INTO ALK

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  • Handelsnavn:
  • MAXX INTO ALK2
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  • Mennesker
  • Medicin typen:
  • Medicinsk udstyr

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Lokation

  • Fås i:
  • MAXX INTO ALK2
    Danmark
  • Sprog:
  • dansk

Andre oplysninger

Status

  • Kilde:
  • Ecolab
  • Autorisationsnummer:
  • 116219E
  • Sidste ændring:
  • 12-03-2018

Produktresumé

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PUNKT 1. IDENTIFIKATION AF STOFFET/ BLANDINGEN OG AF SELSKABET/ VIRKSOMHEDEN

1.1 Produktidentifikator

Produktnavn

MAXX Into Alk2

Produkt kode

116219E

Anvendelse af stoffet/det

kemiske produkt

Sanitært rengøringsmiddel

Stoftype

Blanding

Kun til erhvervsmæssig brug.

Information om fortyndning

Ingen information om fortyndning angivet.

1.2 Relevante identificerede anvendelser for stoffet eller blandingen samt anvendelser, der

frarådes

Identificerede anvendelser

Sanitært rengøringsmiddel. Manuel proces

Sanitært rengøringsmiddel. Spray og aftør, manuel proces

Gulvrengøringsmiddel. Delvis automatisk proces

Anbefalede begrænsninger i

brugen

Forbeholdt industriel og erhvervsmæssig brug.

1.3 Nærmere oplysninger om leverandøren af sikkerhedsdatabladet

Firma

Ecolab ApS

Høffdingsvej 36

2500 Valby, Danmark Tel +45 36 15 85 85

dk-customerservice@ecolab.com

1.4 Nødtelefon

Nødtelefon

36 15 85 85 (hverdage 8.00 - 16.00)

Giftinformationen tlf. nr.

82 12 12 12

Udstedelse-/revisionsdato

27.01.2017

Udgave

PUNKT 2. FAREIDENTIFIKATION

2.1 Klassificering af stoffet eller blandingen

Klassificering (FORORDNING (EF) Nr. 1272/2008)

Ikke et farligt stof eller blanding.,Specifikke koncentrationsgrænser blev anvendt til beregning af

klassificeringen

2.2 Mærkningselementer

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Etikettering (FORORDNING (EF) Nr. 1272/2008)

Ikke et farligt stof eller blanding.

Tillægsmærkning:

Særlig mærkning af visse

blandinger

Sikkerhedsdatablad kan på anmodning rekvireres.

2.3 Andre farer

Ingen kendte.

PUNKT 3. SAMMENSÆTNING AF/ OPLYSNING OM INDHOLDSSTOFFER

3.2 Blandinger

Farlige komponenter

Kemisk betegnelse

CAS-Nr.

EF-Nr.

REACH No.

KlassificeringFORORDNING (EF) Nr.

1272/2008

Koncentration

C8-C10-polyglycosid

68515-73-1

500-220-1

01-2119488530-36

Alvorlig øjenskade Kategori 1; H318

>= 3 - < 5

Natriumcumolsulfonat

28348-53-0

248-983-7

Øjenirritation Kategori 2; H319

>= 1 - < 2.5

For den fuldstændige tekst af faresætningerne nævnt i dette punkt, se punkt 16.

PUNKT 4. FØRSTEHJÆLPSFORANSTALTNINGER

4.1 Beskrivelse af førstehjælpsforanstaltninger

I tilfælde af øjenkontakt

Skyl med rigeligt vand.

I tilfælde af hudkontakt

Skyl med rigeligt vand.

Ved indtagelse.

Skyl munden. Søg læge hvis symptomer opstår.

Hvis det indåndes

Søg læge hvis symptomer opstår.

4.2 Vigtigste symptomer og virkninger, både akutte og forsinkede

I afsnit 11 findes mere detaljerede oplysninger om helbredspåvirkninger og symptomer.

4.3 Angivelse af om øjeblikkelig lægehjælp og særlig behandling er nødvendig

Behandling

Ingen specifikke foranstaltninger identificeret.

PUNKT 5. BRANDBEKÆMPELSE

5.1 Slukningsmidler

Egnede slukningsmidler

Brandslukningsforanstaltningerne skal være hensigtsmæssige i

forhold til lokale omstændigheder og det omgivne miljø.

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Uegnede slukningsmidler

Ingen kendte.

5.2 Særlige farer i forbindelse med stoffet eller blandingen

Specifikke farer ved

brandbekæmpelse

Ikke brandfarligt eller brændbart.

Farlige

forbrændingsprodukter

Nedbrydningsprodukter kan omfatte de følgende materialer:

Carbonoxider

Nitrogenoxider (NOx)

Svovloxider

Fosforholdige oxider

5.3 Anvisninger for brandmandskab

Særlige personlige

værnemidler, der skal bæres

af brandmandskabet

: Brug personligt beskyttelsesudstyr.

Yderligere oplysninger

: Brandrester og forurenet brandslukningsvand skal bortskaffes i

henhold til de lokale regler.

PUNKT 6. FORHOLDSREGLER OVER FOR UDSLIP VED UHELD

6.1 Personlige sikkerhedsforanstaltninger, personlige værnemidler og nødprocedurer

Rådgivning for ikke-

indsatspersonel

Der henvises til beskyttelsesforanstaltninger nævnt i afsnit 7 og 8.

Rådgivning for

indsatspersonel

Hvis særlig beklædning er påkrævet for at håndtere spildet, skal

man være opmærksom på alle oplysninger i punkt 8 om passende

og upassende materialer.

6.2 Miljøbeskyttelsesforanstaltninger

Miljøbeskyttelsesforanstaltnin

Ingen specielle miljømæssige forholdsregler kræves.

6.3 Metoder og udstyr til inddæmning og oprensning

Metoder til oprydning

Stands lækagen, hvis dette er sikkert. Opbevar og opsaml spild

med ikke brændbart absorberende materiale, (f. eks. sand, jord,

moler el. vermikulit) og placer det i affaldsbeholdere i henhold til

de lokale myndigheders forskrifter (se afsnit 13).Skyl rester væk

med vand. Ved store spild, inddæm det spildte materiale eller

saml det op på anden vis, for at sikre at spild ikke når vandveje.

6.4 Henvisning til andre punkter

Se Afsnit 1 for kontaktoplysninger i nødsituationer.

For personlig beskyttelse se punkt 8.

Se Afsnit 13 for yderligere oplysninger om affaldshåndtering.

PUNKT 7. HÅNDTERING OG OPBEVARING

7.1 Forholdsregler for sikker håndtering

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Råd om sikker håndtering

Vask hænder efter håndtering. For personlig beskyttelse se punkt

Hygiejniske foranstaltninger

Vask hænder før pauser og straks efter håndtering af produktet.

7.2 Betingelser for sikker opbevaring, herunder eventuel uforenelighed

Krav til lager og beholdere

Opbevares utilgængeligt for børn. Hold beholderen tæt lukket.

Opbevares i behørigt mærkede beholdere.

Opbevaringstemperatur

0 °C til 40 °C

7.3 Særlige anvendelser

Særlige anvendelser

Sanitært rengøringsmiddel. Manuel proces

Sanitært rengøringsmiddel. Spray og aftør, manuel proces

Gulvrengøringsmiddel. Delvis automatisk proces

PUNKT 8. EKSPONERINGSKONTROL/PERSONLIGE VÆRNEMIDLER

8.1 Kontrolparametre

Indeholder ingen stoffer med grænseværdi for erhvervsmæssig eksponering.

8.2 Eksponeringskontrol

Passende tekniske foranstaltninger

Tekniske foranstaltninger

God generel ventilation skulle være tilstrækkeligt til at kontrollere

arbejdernes udsættelse for luftbårne urenheder.

Individuelle beskyttelsesforanstaltninger

Hygiejniske foranstaltninger

Vask hænder før pauser og straks efter håndtering af produktet.

Beskyttelse af øjne / ansigt

(EN 166)

Intet specielt beskyttelsesudstyr nødvendigt.

Beskyttelse af hænder (EN

374)

Intet specielt beskyttelsesudstyr nødvendigt.

Beskyttelse af hud og krop

(EN 14605)

Intet specielt beskyttelsesudstyr nødvendigt.

Åndedrætsværn (EN 143,

14387)

Ingen påkrævet, hvis luftbårne koncentrationer holdes under de

oplyste grænseværdier for eksponering. Brug certificerede

åndedrætsværn der opfylder EU-krav (89/656 / EØF, 89/686 /

EØF) eller tilsvarende, når respiratoriske risici ikke kan undgås

eller i tilstrækkelig grad begrænses ved kollektive tekniske

beskyttelsesforanstaltninger eller ved foranstaltninger, metoder

eller procedurer i tilrettelæggelse af arbejdet.

Foranstaltninger til begrænsning af eksponering af miljøet

Generelle anvisninger

: Overvej om det er nødvendig at lukke opbevaringsbeholderne

inde.

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PUNKT 9. FYSISKE OG KEMISKE EGENSKABER

9.1 Oplysninger om grundlæggende fysiske og kemiske egenskaber

Udseende

: væske

Farve

: lysorange

Lugt

: behagelig

pH-værdi

10.7 - 11.3, 100 %

Flammepunkt

Ikke anvendelig

Lugttærskel

Ikke anvendelig og/eller ikke bestemt for blandingen

Smeltepunkt/frysepunkt

Ikke anvendelig og/eller ikke bestemt for blandingen

Begyndelseskogepunkt og

kogepunktsinterval

Ikke anvendelig og/eller ikke bestemt for blandingen

Fordampningshastighed

Ikke anvendelig og/eller ikke bestemt for blandingen

Antændelighed (fast stof,

luftart)

Ikke anvendelig og/eller ikke bestemt for blandingen

Højeste eksplosionsgrænse

Ikke anvendelig og/eller ikke bestemt for blandingen

Laveste eksplosionsgrænse

Ikke anvendelig og/eller ikke bestemt for blandingen

Damptryk

Ikke anvendelig og/eller ikke bestemt for blandingen

Relativ dampvægtfylde

Ikke anvendelig og/eller ikke bestemt for blandingen

Relativ massefylde

1.13 - 1.17

Vandopløselighed

opløselig

Opløselighed i andre

opløsningsmidler

Ikke anvendelig og/eller ikke bestemt for blandingen

Fordelingskoefficient: n-

oktanol/vand

Ikke anvendelig og/eller ikke bestemt for blandingen

Selvantændelsestemperatur

Ikke anvendelig og/eller ikke bestemt for blandingen

Termisk spaltning

Ikke anvendelig og/eller ikke bestemt for blandingen

Viskositet, kinematisk

Ikke anvendelig og/eller ikke bestemt for blandingen

Eksplosive egenskaber

Ikke anvendelig og/eller ikke bestemt for blandingen

Oxiderende egenskaber

Stoffet eller blandingen er ikke klassificeret som oxiderende.

9.2 Andre oplysninger

Ikke anvendelig og/eller ikke bestemt for blandingen

PUNKT 10. STABILITET OG REAKTIVITET

10.1 Reaktivitet

Ingen farlige reaktioner kendt ved normalt brug under normale forhold.

10.2 Kemisk stabilitet

Stabil under normale forhold.

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10.3 Risiko for farlige reaktioner

Ingen farlige reaktioner kendt ved normalt brug under normale forhold.

10.4 Forhold, der skal undgås

Ingen kendte.

10.5 Materialer, der skal undgås

Ingen kendte.

10.6 Farlige nedbrydningsprodukter

Nedbrydningsprodukter kan omfatte de følgende materialer:

Carbonoxider

Nitrogenoxider (NOx)

Svovloxider

Fosforholdige oxider

PUNKT 11. TOKSIKOLOGISKE OPLYSNINGER

11.1 Oplysninger om toksikologiske virkninger

Oplysninger om sandsynlige

eksponeringsveje

Indånding, Øjenkontakt, Hudkontakt

Produkt

Akut oral toksicitet

: Der er ingen tilgængelige data på dette produkt.

Akut toksicitet ved indånding

: Der er ingen tilgængelige data på dette produkt.

Akut dermal toksicitet

: Der er ingen tilgængelige data på dette produkt.

Hudætsning/-irritation

: Der er ingen tilgængelige data på dette produkt.

Alvorlig

øjenskade/øjenirritation

: Der er ingen tilgængelige data på dette produkt.

Respiratorisk sensibilisering

eller hudsensibilisering

: Der er ingen tilgængelige data på dette produkt.

Kræftfremkaldende

egenskaber

: Der er ingen tilgængelige data på dette produkt.

Reproduktionsskadende

virkninger

: Der er ingen tilgængelige data på dette produkt.

Kimcellemutagenicitet

: Der er ingen tilgængelige data på dette produkt.

Fosterbeskadigelse

: Der er ingen tilgængelige data på dette produkt.

Enkel STOT-eksponering

: Der er ingen tilgængelige data på dette produkt.

Gentagne STOT-

: Der er ingen tilgængelige data på dette produkt.

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eksponeringer

Aspiration giftighed

: Der er ingen tilgængelige data på dette produkt.

Komponenter

Akut oral toksicitet

: C8-C10-polyglycosid

LD50 Rotte: > 5,000 mg/kg

Natriumcumolsulfonat

LD50 Rotte: > 7,000 mg/kg

Komponenter

Akut toksicitet ved indånding

: Natriumcumolsulfonat

4 h LC50 Rotte: > 770 mg/l

Komponenter

Akut dermal toksicitet

: C8-C10-polyglycosid

LD50 Kanin: > 2,000 mg/kg

Natriumcumolsulfonat

LD50 Kanin: > 2,000 mg/kg

Potentielle sundhedspåvirkninger

Øjne

Helbredsskader er ikke kendte eller forventede ved normalt brug.

Helbredsskader er ikke kendte eller forventede ved normalt brug.

Indtagelse

Helbredsskader er ikke kendte eller forventede ved normalt brug.

Indånding

Helbredsskader er ikke kendte eller forventede ved normalt brug.

Langtidspåvirkning

Helbredsskader er ikke kendte eller forventede ved normalt brug.

Erfaringer med human eksponering

Øjenkontakt

Ingen kendte eller forventede symptomer.

Hudkontakt

Ingen kendte eller forventede symptomer.

Indtagelse

Ingen kendte eller forventede symptomer.

Indånding

Ingen kendte eller forventede symptomer.

PUNKT 12. MILJØOPLYSNINGER

12.1 Økotoksicitet

Miljøpåvirkninger

Dette produkt har ingen kendt økotoksikologisk effekt.

Produkt

Toksicitet overfor fisk

: Ingen data tilgængelige

Toksicitet for dafnier og

andre hvirvelløse vanddyr.

: Ingen data tilgængelige

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Toksicitet overfor alger

: Ingen data tilgængelige

Komponenter

Toksicitet overfor fisk

: Natriumcumolsulfonat

96 h LC50 Fisk: > 450 mg/l

Komponenter

Toksicitet overfor alger

: C8-C10-polyglycosid

72 h EC50: 18 mg/l

12.2 Persistens og nedbrydelighed

Produkt

Biologisk nedbrydelighed

: Tensiderne i produktet er biologisk nedbrydelige iht. kravene i

forordning nr. 648/2004 om vaske- og rengøringsmidler.

Komponenter

Biologisk nedbrydelighed

C8-C10-polyglycosid

Resultat: Let bionedbrydeligt.

Natriumcumolsulfonat

Resultat: Let bionedbrydeligt.

12.3 Bioakkumuleringspotentiale

Ingen data tilgængelige

12.4 Mobilitet i jord

Ingen data tilgængelige

12.5 Resultater af PBT- og vPvB-vurdering

Produkt

Vurdering

Dette stof/blanding indeholder ingen komponenter, der anses for

at være enten persistente, bioakkumulerende og toksiske (PBT)

eller meget persistente og meget bioakkumulerende (vPvB) ved

niveauer på 0.1% eller højere.

12.6 Andre negative virkninger

Ingen data tilgængelige

PUNKT 13. BORTSKAFFELSE

Bortskaffes i overensstemmelse med EU-direktiverne om affald og farligt affald.Affaldskoder skal

fastsættes af bruger, at fortrække i samarbejde med de myndigheder der er ansvarlig for

bortskaffelse af affald.

13.1 Metoder til affaldsbehandling

Produkt

: Hvor det er muligt foretrækkes genanvendelse frem for

bortskaffelse eller forbrænding. Hvis genanvendelse ikke er

praktisk muligt, skal bortskaffelse ske i henhold til lokale

regulativer. Bortskaf affald til en godkendt

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affaldsbortskaffelsesfacilitet.

Fortyndet produkt kan skylles til sanitære kloaksystem

Forurenet emballage

: Bortskaffes i overensstemmelse med lokale, regionale og

nationale bestemmelser.

Vejledning til valg af

affaldskoder

: Organisk affald indeholdende farlige stoffer. Hvis dette produkt

anvendes i yderligere processer, skal den endelige bruger

omdefinere og tildele den mest hensigtsmæssige Europæiske

Affaldskatalogkode (EAK). Det påhviler den der producerer

affaldet at bestemme toksicitet og fysiske egenskaber af

materialet som genereres for at identificere affaldet korrekt og

bestemme bortskaffelsemetoder af affaldet i overensstemmelse

med gældende europæisk (EU direktiv 2008/98 / EF) og lokale

bestemmelser.

PUNKT 14. TRANSPORTOPLYSNINGER

Afsenderen har ansvar for, at emballager, etikettering og mærkning er i overensstemmelse med den

valgte transportform.

Vejtransport (ADR/ADN/RID)

14.1 FN-nummer

Ikke farligt gods

14.2 UN-

forsendelsesbetegnelse (UN

proper shipping name)

Ikke farligt gods

14.3 Transportfareklasse( r )

Ikke farligt gods

14.4 Emballagegruppe

Ikke farligt gods

14.5 Miljøfarer

Ikke farligt gods

14.6 Særlige

forsigtighedsregler for

brugeren

Ikke farligt gods

Lufttransport (IATA)

14.1 FN-nummer

Ikke farligt gods

14.2 UN-

forsendelsesbetegnelse (UN

proper shipping name)

Ikke farligt gods

14.3 Transportfareklasse( r )

Ikke farligt gods

14.4 Emballagegruppe

Ikke farligt gods

14.5 Miljøfarer

Ikke farligt gods

14.6 Særlige

forsigtighedsregler for

brugeren

Ikke farligt gods

Søtransport (IMDG/IMO)

14.1 FN-nummer

Ikke farligt gods

14.2 UN-

forsendelsesbetegnelse (UN

proper shipping name)

Ikke farligt gods

14.3 Transportfareklasse( r )

Ikke farligt gods

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14.4 Emballagegruppe

Ikke farligt gods

14.5 Miljøfarer

Ikke farligt gods

14.6 Særlige

forsigtighedsregler for

brugeren

Ikke farligt gods

14.7 Bulktransport i henhold

til bilag II til MARPOL 73/78

og IBC-koden

Ikke farligt gods

PUNKT 15. OPLYSNINGER OM REGULERING

15.1 Særlige bestemmelser/særlig lovgivning for stoffet eller blandingen med hensyn til

sikkerhed, sundhed og miljø

iht. Detergent Forordningen

EU 648/2004

under 5 %: Anioniske overfladeaktive stoffer, Nonioniske

overfladeaktive stoffer

Andre bestanddele: Parfume

Allergener:

d-Limonen

National lovgivning

Vær opmærksom på Dir 94/33/EF til beskyttelse af unge mennesker på arbejde.

Produktregister nummer

2485655

15.2 Kemikaliesikkerhedsvurdering

Produktet indeholder stoffer, for hvilke der fortsat kræves en kemisk sikkerhedsvurdering.

PUNKT 16. ANDRE OPLYSNINGER

Procedure anvendt til at bestemme klassificeringen i henhold til

FORORDNING (EF) Nr. 1272/2008

Klassifikation

Begrundelse

Ikke et farligt stof eller blanding.

Beregningsmetoden

Fuld tekst af H-sætninger

H318

Forårsager alvorlig øjenskade.

H319

Forårsager alvorlig øjenirritation.

Fuld tekst af andre forkortelser

ADN - Europæisk konvention om international transport af farligt gods ad indre vandveje; ADR -

Europæisk konvention om international transport af farligt gods ad vej; AICS

- Australiens

fortegnelse over kemiske stoffer; ASTM - Det amerikanske forbund for testning af materialer,

ASTM; bw - Kropsvægt; CLP - CLP-forordningen om klassificering, mærkning og emballering;

Forordning (EF) Nr. 1272/2008; CMR - Kræftfremkaldende, mutagent eller reproduktionstoksisk

stof; DIN - Standard fra det tyske standardiseringsinstitut; DSL - Liste over indenlandske stoffer

(Canada);

ECHA

europæiske

kemikalieagentur;

EC-Number

EU-nummer;

Koncentration forbundet med x % respons; ELx - Belastningsgrad forbundet med x % respons;

EmS - Nødplan; ENCS - Eksisterende og nye kemiske stoffer (Japan); ErCx - Koncentration

forbundet med x % vækstrate respons; GHS - Det globale harmoniserede system; GLP - God

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laboratoriepraksis;

IARC

Internationale

Agentur

Kræftforskning;

IATA

Internationale Luftfartssammenslutning, IATA; IBC - Den internationale kode for konstruktion og

udrustning af skibe, som fører farlige kemikalier i bulk; IC50 - Halv maksimal inhiberende

koncentration; ICAO - Organisationen for International Civil Luftfart, ICAO; IECSC - Fortegnelse

over eksisterende kemikalier i Kina; IMDG - Det internationale regelsæt for søtransport af farligt

gods; IMO - Den Internationale Søfartsorganisation; ISHL - Lov om industriel sikkerhed og

sundhed (Japan); ISO - International standardiseringsorganisation; KECI - Koreas fortegnelse

over eksisterende kemikalier; LC50 - Dødelig koncentration for 50 % af en testpopulation; LD50 -

Dødelig dosis for 50 % af en testpopulation (gennemsnitlig dødelig dosis); MARPOL - Den

internationale konvention om forebyggelse af forurening fra skibe; n.o.s. - Andet ikke angivet;

NO(A)EC - Koncentration for ingen observeret (negativ) virkning; NO(A)EL - Niveau for ingen

observeret (negativ) virkning; NOELR - Belastningsgrad for ingen observeret virkning; NZIoC -

New Zealands fortegnelse over kemikalier; OECD - Organisationen for Økonomisk Samarbejde

og Udvikling; OPPTS - Afdelingen for kemisk sikkerhed og forebyggelse af forurening; PBT -

Persistent, bioakkumulativt og giftigt stof; PICCS - Fillippinernes fortegnelse over kemikalier og

kemiske stoffer; (Q)SAR - (Kvantitativt) forhold mellem struktur og aktivitet; REACH - Europa-

parlamentets og Rådets forordning (EF) nr. 1272/2008 om registrering, vurdering og godkendelse

af samt begrænsninger for kemikalier; RID - Reglement for international befordring af farligt gods

med jernbane; SADT - Selvaccelererende dekompositionstemperatur; SDS - Sikkerhedsdatablad;

TCSI - Taiwans fortegnelse over kemiske stoffer; TRGS - Teknisk forskrift for farlige stoffer; TSCA

- Lov om kontrol af giftige stoffer (USA); UN - Forenede Nationer; vPvB - Meget persistent og

meget bioakkumulativ

Udarbejdet af

Regulatory Affairs

Tal angives i sikkerhedsdatabladet i følgende form: 1,000,000 = 1 million og 1,000 = 1 tusind. 0.1

= 1 tiendedel og 0.001 = 1 tusindedel.

REVIDERET INFORMATION: Signifikante ændringer i den regulatoriske eller sundhedsmæssige

information af denne revision er angivet med en lodret streg i sikkerhedsdatabladets venstre

margin.

Informationerne i dette Arbejdshygiejniske Datablad er efter vor bedste viden, oplysninger og

overbevisning korrekte på datoen, hvor det er trykt. Informationerne tjener kun som vejledning til

sikker håndtering, brug, forarbejdning, lagring, transport, disponering og frigivelse og kan ikke

betragtes som en garanti eller kvalitetsangivelse. Informationerne vedrører kun det udtrykkeligt

angivne materiale og er ikke gældende for dette materiale anvendt i kombination med andre

materialer eller forarbejdning, medmindre udtrykkeligt anført i teksten.

BILAG: EKSPONERINGSSCENARIER

DPD+-stoffer

:

Følgende stoffer er de vigtigste stoffer der bidrager til blandingens eksponeringsscenarie i henhold

til DPD+-regelen:

Måde for

optagelse

Stof

CAS-Nr.

EINECS-Nr.

Indtagelse

Ikke afhængighedsstof

Indånding

Ikke afhængighedsstof

C8-C10-polyglycosid

68515-73-1

500-220-1

Øjne

C8-C10-polyglycosid

68515-73-1

500-220-1

SIKKERHEDSDATABLAD

i henhold til Forordning (EF) nr. 1907/2006

MAXX Into Alk2

116219E

12 / 13

vandmiljø

Ikke afhængighedsstof

For at beregne om anvendelsesforholdene og de nødvendige risikohåndteringsforanstaltninger

er sikre, venligst kalkuler risikofaktor på dette web site:

www.ecetoc.org/tra

Eksponeringsscenariets korte

titel

Sanitært rengøringsmiddel. Manuel proces

Use descriptors

Hovedbrugergrupper

Faglige anvendelser: Det offentlige område (administration,

uddannelse, forlystelser, tjeneste-ydelser, håndværkere)

Slutanvendelsessektor

SU22: Faglige anvendelser: Det offentlige område (administration,

uddannelse, forlystelser, tjeneste-ydelser, håndværkere)

Proceskategorier

PROC10: Påføring med rulle eller pensel

PROC8a: Overførsel af stof eller kemisk produkt (påfyldning/

udtømning) fra/ til kar/ store beholdere på ikke-dedikerede anlæg

Produktkategorier

PC35: Vaske- og renseprodukter (herunder opløsnings-

middelbaserede produkter)

Miljøudledningskategorier

ERC8a: Udbredt indendørs anvendelse af proceshjælpemidler i

åbne systemer

Eksponeringsscenariets korte

titel

Sanitært rengøringsmiddel. Spray og aftør, manuel proces

Use descriptors

Hovedbrugergrupper

Faglige anvendelser: Det offentlige område (administration,

uddannelse, forlystelser, tjeneste-ydelser, håndværkere)

Slutanvendelsessektor

SU22: Faglige anvendelser: Det offentlige område (administration,

uddannelse, forlystelser, tjeneste-ydelser, håndværkere)

Proceskategorier

PROC10: Påføring med rulle eller pensel

PROC11: Ikke-industriel sprøjtning

PROC8a: Overførsel af stof eller kemisk produkt (påfyldning/

udtømning) fra/ til kar/ store beholdere på ikke-dedikerede anlæg

Produktkategorier

PC35: Vaske- og renseprodukter (herunder opløsnings-

middelbaserede produkter)

Miljøudledningskategorier

ERC8a: Udbredt indendørs anvendelse af proceshjælpemidler i

åbne systemer

SIKKERHEDSDATABLAD

i henhold til Forordning (EF) nr. 1907/2006

MAXX Into Alk2

116219E

13 / 13

Eksponeringsscenariets korte

titel

Gulvrengøringsmiddel. Delvis automatisk proces

Use descriptors

Hovedbrugergrupper

Faglige anvendelser: Det offentlige område (administration,

uddannelse, forlystelser, tjeneste-ydelser, håndværkere)

Slutanvendelsessektor

SU22: Faglige anvendelser: Det offentlige område (administration,

uddannelse, forlystelser, tjeneste-ydelser, håndværkere)

Proceskategorier

PROC10: Påføring med rulle eller pensel

PROC8a: Overførsel af stof eller kemisk produkt (påfyldning/

udtømning) fra/ til kar/ store beholdere på ikke-dedikerede anlæg

Produktkategorier

PC35: Vaske- og renseprodukter (herunder opløsnings-

middelbaserede produkter)

Miljøudledningskategorier

ERC8a: Udbredt indendørs anvendelse af proceshjælpemidler i

åbne systemer

  • Oplysningerne indlægssedlen for dette produkt er i øjeblikket ikke tilgængelig, kan du sende en anmodning til vores kundeservice, og vi vil give dig besked, så snart vi er i stand til at opnå det.

    Anmode informationsbrochure for offentligheden.



  • Dokumenter på andre sprog er tilgængelige her

19-4-2018

NxtGen Botanicals Maeng Da Kratom by NGB Corp.: Recall - Possible Salmonella Contamination

NxtGen Botanicals Maeng Da Kratom by NGB Corp.: Recall - Possible Salmonella Contamination

NGB Corp. of West Jordan, Utah is voluntarily recalling NxtGen Botanicals Maeng Da Kratom labeled bottles of encapsulated product because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infec...

FDA - U.S. Food and Drug Administration

19-4-2018

Certain Kratom-Containing Powder Products by Viable Solutions: Recall -Possible Salmonella Contamination

Certain Kratom-Containing Powder Products by Viable Solutions: Recall -Possible Salmonella Contamination

Viable Solutions of Nampa, ID has initiated a recall of certain Kratom-containing powder products, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result...

FDA - U.S. Food and Drug Administration

18-4-2018

24-Hour Multi-Patient Use Endoscope Connectors: Letter to HealthCare Providers and Healthcare Facilities - Risk of Cross-Contamination

24-Hour Multi-Patient Use Endoscope Connectors: Letter to HealthCare Providers and Healthcare Facilities - Risk of Cross-Contamination

the recommended instructions and device design for the ERBEFLO port connector do not adequately mitigate the risks of cross-contamination for endoscopy patients. This is because the connector, tubing, and/or water bottle can become contaminated with blood, stool, or other fluids from previous patients that travel back through the endoscope channels into the connector and tubing. Endoscope connectors that are labeled for use with multiple patients over the course of 24 hours without reprocessing are kno...

FDA - U.S. Food and Drug Administration

15-4-2018

K9 Natural Ltd Voluntarily Recalls K9 Natural Frozen Chicken Feast Raw Pet Food 2.2lb And 11lb Bags Because Of Possible <em>Listeria Monocytogenes</em>

K9 Natural Ltd Voluntarily Recalls K9 Natural Frozen Chicken Feast Raw Pet Food 2.2lb And 11lb Bags Because Of Possible <em>Listeria Monocytogenes</em>

K9 Natural Ltd is voluntarily recalling four batches of the K9 Natural Frozen Chicken Feast 2.2lb and 11lb bags that was imported into the US market in June 2017 because they have the potential to be contaminated with Listeria Monocytogenes.

FDA - U.S. Food and Drug Administration

14-4-2018

Rose Acre Farms Recalls Shell Eggs Due to Possible Health Risk

Rose Acre Farms Recalls Shell Eggs Due to Possible Health Risk

Through an abundance of caution Rose Acre Farms of Seymour, Indiana is voluntarily recalling 206,749,248 eggs because they have the potential to be contaminated with Salmonella Braenderup, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals infected with Salmonella Braenderup can experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmo...

FDA - U.S. Food and Drug Administration

11-4-2018

Premier Pharmacy Labs Issues Voluntary Nationwide Recall of Specific Sterile Injectable Products Lots Due to a Potential Lack of Sterility Assurance

Premier Pharmacy Labs Issues Voluntary Nationwide Recall of Specific Sterile Injectable Products Lots Due to a Potential Lack of Sterility Assurance

Microbial contamination was detected during routine testing of subsequent unreleased product lots due to interaction between the product syringe and tamper evident container closure, which may result in the potential introduction of microorganisms into the products.

FDA - U.S. Food and Drug Administration

9-4-2018

Club 13 Recalls Kratom Maeng Da Red Powder and Capsules Because of Possible Health Risk

Club 13 Recalls Kratom Maeng Da Red Powder and Capsules Because of Possible Health Risk

Club 13 of St. Augustine, FL is recalling 15-gram, 30-gram, 90-gram, 150-gram, and 454-gram pouches, and all bulk orders of "Maeng Da Red" kratom powder; and 5-count, 25-count, 50-count, 100-count, 120-count capsule, and all bulk capsule orders of “Maeng Da Red” kratom bottles; and 5-count, 20-count, 25-count, 40-count, 50-count capsule “Maeng Da Red XS” kratom bottles because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections i...

FDA - U.S. Food and Drug Administration

5-4-2018

Global Commodities Corporation Recalls Buenas Grated Coconut due to Possible Health Risk

Global Commodities Corporation Recalls Buenas Grated Coconut due to Possible Health Risk

Global Commodities Corporation, Hayward, CA is recalling one lot of Buenas Brand frozen grated coconut because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can...

FDA - U.S. Food and Drug Administration

30-3-2018

Health Nut Factory Recalls Organic Coconut Smiles Because Of Possible Health Risk

Health Nut Factory Recalls Organic Coconut Smiles Because Of Possible Health Risk

Healthy Nut Factory of Bayside, NY is recalling 7 oz. Pouches of Organic Coconut Smiles because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the org...

FDA - U.S. Food and Drug Administration

29-3-2018

Federal judge approves consent decree with New York dietary supplement manufacturer Riddhi USA

Federal judge approves consent decree with New York dietary supplement manufacturer Riddhi USA

A New York dietary supplement manufacturer has been ordered by a federal court to stop selling its products until the company comes into compliance with the FDA’s dietary supplement manufacturing regulations.

FDA - U.S. Food and Drug Administration

25-3-2018

Tamarack Inc. Recalls Eclipse Kratom Because of Possible Salmonella Contamination

Tamarack Inc. Recalls Eclipse Kratom Because of Possible Salmonella Contamination

Tamarack Inc. of Roy, Utah is voluntarily recalling Eclipse Kratom-containing powder products because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in t...

FDA - U.S. Food and Drug Administration

22-3-2018

Statement from FDA’s Donald St. Pierre on findings from ongoing investigation into lead testing issues

Statement from FDA’s Donald St. Pierre on findings from ongoing investigation into lead testing issues

FDA on findings from ongoing investigation into lead testing issues; studies find chemical interaction during test processing may contribute to skewing results

FDA - U.S. Food and Drug Administration

19-3-2018

Natural Grocers Issues Recall on Coconut Smiles Organic Due to <em>Salmonella</em>

Natural Grocers Issues Recall on Coconut Smiles Organic Due to <em>Salmonella</em>

Vitamin Cottage Natural Food Markets, Inc., a Lakewood, Colorado-based natural grocery chain, is recalling Natural Grocers brand 10-ounce Coconut Smiles Organic due to the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rar...

FDA - U.S. Food and Drug Administration

18-3-2018

Medical Devices Safety Update Volume 6, Number 2, March 2018

Medical Devices Safety Update Volume 6, Number 2, March 2018

Preventable alarm issues; Review into cochlear implants; NHS cylinder alert; recent safety alerts

Therapeutic Goods Administration - Australia

17-3-2018

International Harvest, Inc. Recalls Organic Go Smile! Raw Coconut Because of Possible Health Risk

International Harvest, Inc. Recalls Organic Go Smile! Raw Coconut Because of Possible Health Risk

International Harvest, Inc of Mount Vernon, NY is recalling 14,620 lbs. of bulk and 24,270 bags of Organic Go Smile! Raw Coconut, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infec...

FDA - U.S. Food and Drug Administration

17-3-2018

River Valley Sprouts Recalls Alfalfa Sprouts and Garlic Alfalfa Sprouts Due to Possible Salmonella Contamination

River Valley Sprouts Recalls Alfalfa Sprouts and Garlic Alfalfa Sprouts Due to Possible Salmonella Contamination

River Valley Sprouts is voluntarily recalling its 5 ounce Alfalfa Sprouts, 4 ounce Alfalfa Sprouts, 5 ounce Garlic/Alfalfa and 5 ounce Variety sprouts because they have the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail, elderly people, and others with weakened immune systems. Healthy persons often experience fever, diarrhea, nausea, vomiting and abdominal pain. In rare circumstances, infection with salmonella can ...

FDA - U.S. Food and Drug Administration

16-3-2018

Tobacco and related products

Tobacco and related products

The Tobacco Products Directive (2014/40/EU) lays down rules relating to the manufacture, presentation and sale of tobacco and related products (other smoking products, vaping products). While it does not establish a marketing authorisation system, the Directive requires manufacturers and importers to declare these products to the competent authorities of the Member States before they can be marketed. Their composition, emissions, toxicological data on the ingredients, in-depth studies for certain additiv...

France - Agence Nationale du Médicament Vétérinaire

12-3-2018

Traces of chemical contaminants in food – three questions for Roger Genet

Traces of chemical contaminants in food – three questions for Roger Genet

Roger Genet, Director General of ANSES, considers the issue of chemical contaminants in fruit and vegetables, which does not necessarily translate into a risk for the consumer. He explains how the Agency goes about monitoring the presence of pesticide residues in food, assessing the exposure of different population groups and ensuring consumer protection.   Language English

France - Agence Nationale du Médicament Vétérinaire

7-3-2018

March 6, 2018: Monterey Park Woman Sentenced to Two Years in Prison for Injecting Foreign Substance into Woman for Buttocks Enhancement

March 6, 2018: Monterey Park Woman Sentenced to Two Years in Prison for Injecting Foreign Substance into Woman for Buttocks Enhancement

March 6, 2018: Monterey Park Woman Sentenced to Two Years in Prison for Injecting Foreign Substance into Woman for Buttocks Enhancement

FDA - U.S. Food and Drug Administration

6-3-2018

InSinkErator recalls Single Outlet Sink Top Switch

InSinkErator recalls Single Outlet Sink Top Switch

Water can get into the power module, posing a potential fire hazard.

Health Canada

7-2-2018

Pentax Medical Duodenoscope Model ED-3490TK: FDA Safety Communication -  Updated Design and Labeling Cleared

Pentax Medical Duodenoscope Model ED-3490TK: FDA Safety Communication - Updated Design and Labeling Cleared

Design changes are intended to reduce the potential for leakage of patient fluids into the closed elevator channel and under the distal cap.

FDA - U.S. Food and Drug Administration

31-1-2018

AirLife Humidification Chamber, Heated Breathing Circuit Kits by Vyaire Medical: Class I Recall - Manufacturing Error

AirLife Humidification Chamber, Heated Breathing Circuit Kits by Vyaire Medical: Class I Recall - Manufacturing Error

Parts of the chamber may split apart into layers, allowing water to overflow the chamber and back up into the patient breathing circuit, which could lead to serious adverse health consequences, including injury or death.

FDA - U.S. Food and Drug Administration

11-1-2018

FDA warns Becton Dickinson & Company of significant violations of the law as part of ongoing investigation into lead testing issues

FDA warns Becton Dickinson & Company of significant violations of the law as part of ongoing investigation into lead testing issues

FDA warns Becton Dickinson & Company of significant violations of the law as part of ongoing investigation into lead testing issues

FDA - U.S. Food and Drug Administration

2-1-2018

Reprocessed Agilis Steerable Introducer Sheath by Sterilmed: Class I Recall - Improper Seal of Sheath Hub

Reprocessed Agilis Steerable Introducer Sheath by Sterilmed: Class I Recall - Improper Seal of Sheath Hub

Improper seals can allow blood to leak through the hub, cause the cap to fall off during the procedure, or can create a difference in pressure that allows air into the circulatory system (air embolism).

FDA - U.S. Food and Drug Administration

5-12-2017

NETGEAR, Inc. recalls Power Adapter for Arlo Pro Outdoor Cameras

NETGEAR, Inc. recalls Power Adapter for Arlo Pro Outdoor Cameras

Water can leak into the weatherproof connector on the power adapter and cause a short circuit, melting, and overheating, posing a fire hazard.

Health Canada

28-11-2017

TGA actions after review into urogynaecological surgical mesh implants

TGA actions after review into urogynaecological surgical mesh implants

TGA undertakes regulatory actions after review into urogynaecological surgical mesh implants

Therapeutic Goods Administration - Australia

27-11-2017

November 22, 2017: Former Pharmacy Compliance Director Pleads Guilty to Introducing Adulterated Drugs into Interstate Commerce and Conspiracy to Defraud the United States

November 22, 2017: Former Pharmacy Compliance Director Pleads Guilty to Introducing Adulterated Drugs into Interstate Commerce and Conspiracy to Defraud the United States

November 22, 2017: Former Pharmacy Compliance Director Pleads Guilty to Introducing Adulterated Drugs into Interstate Commerce and Conspiracy to Defraud the United States

FDA - U.S. Food and Drug Administration

15-11-2017

Benefit Cosmetics Services Canada Inc. recalls Gimme Brow Volumizing Eyebrow Gel

Benefit Cosmetics Services Canada Inc. recalls Gimme Brow Volumizing Eyebrow Gel

Routine quality testing identified that some of the recalled product is contaminated with Pseudomonas aeruginosa. If introduced into the eye through accidental contact, this poses a risk of causing infections in individuals with compromised or weakened immune systems.

Health Canada

14-11-2017

Injectable Silicone for Body Contouring and Enhancement: FDA Safety Communication - FDA Warns Against Use

Injectable Silicone for Body Contouring and Enhancement: FDA Safety Communication - FDA Warns Against Use

Silicone, when injected into areas with many blood vessels, can travel to other parts of the body and block blood vessels in the lungs, heart, or brain. This can result in permanent damage to those tissues and lead to stroke or death.

FDA - U.S. Food and Drug Administration

14-11-2017

Filling in Wrinkles Safely

Filling in Wrinkles Safely

In the quest for youthful looks, both men and women are seeking treatments to minimize laugh lines and other wrinkles. Learn about a popular treatment that involves injecting dermal fillers into the face, its benefits and risks.

FDA - U.S. Food and Drug Administration

31-10-2017

October 31, 2017: South Korean Maker of Contact Lenses, Company CEO Charged with Smuggling Products into U.S. by Failing to Declare Full Value

October 31, 2017: South Korean Maker of Contact Lenses, Company CEO Charged with Smuggling Products into U.S. by Failing to Declare Full Value

October 31, 2017: South Korean Maker of Contact Lenses, Company CEO Charged with Smuggling Products into U.S. by Failing to Declare Full Value

FDA - U.S. Food and Drug Administration

25-10-2017

Relish Foods, Inc. Recalls Frozen Tuna Loins Because of Possible Health Risk

Relish Foods, Inc. Recalls Frozen Tuna Loins Because of Possible Health Risk

On October 13, 2017, Relish Foods, Inc. of Culver City, Calif., voluntarily initiated the recall of frozen Newport brand 5 to 8 lb. tuna loins. The recall has since expanded to include: 3 to 5 lb. tuna loins, 6 oz. tuna steaks, and 4 oz. tuna steaks. The recall is the result of sampling by the FDA which revealed that the product has potential to contain the bacteria Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with w...

FDA - U.S. Food and Drug Administration

23-10-2017

FDA warns Magellan Diagnostics of significant violations of the law as part of investigation into lead testing issues

FDA warns Magellan Diagnostics of significant violations of the law as part of investigation into lead testing issues

Today the U.S. Food and Drug Administration issued a warning letter to Magellan Diagnostics Inc. for several violations of federal law, including marketing significantly modified versions of two of its blood lead testing systems without the FDA’s required clearance or approval and failing to submit medical device reports to the FDA after becoming aware of customer complaints involving discrepancies in blood lead test results.

FDA - U.S. Food and Drug Administration

13-10-2017

California dietary supplement maker, Custompax prohibited from manufacturing

California dietary supplement maker, Custompax prohibited from manufacturing

A California dietary supplement manufacturer recently was ordered by a federal court to stop selling its products until the company comes into compliance with the U.S. Food and Drug Administration’s dietary supplement manufacturing regulations and other requirements listed in a consent decree.

FDA - U.S. Food and Drug Administration

4-10-2017

ANSES celebrates science

ANSES celebrates science

The annual Fête de la Science (Science Festival) is the ideal event for promoting scientific research and its various professions. As a health agency with eleven research and reference laboratories, ANSES participates fully in this festival, giving the public a special insight into the work of its scientists and their passion for science devoted to health and safety. Various events will thus be on offer all over France from 6 to 15 October 2017, enabling the population to discover or rediscover ANSES's e...

France - Agence Nationale du Médicament Vétérinaire

4-10-2017

X-Lite Corporation recalls Du MAURIER Cigarette Case with Built-in Lighter

X-Lite Corporation recalls Du MAURIER Cigarette Case with Built-in Lighter

The lighter built into the cigarette case can be misused, posing a burn hazard to consumers.

Health Canada

2-10-2017

September 29, 2017: Randallstown Woman Sentenced To 2 Years In Prison For Injecting Non-Medical Grade Silicone Into The Bodies Of Victim Customers

September 29, 2017: Randallstown Woman Sentenced To 2 Years In Prison For Injecting Non-Medical Grade Silicone Into The Bodies Of Victim Customers

September 29, 2017: Randallstown Woman Sentenced To 2 Years In Prison For Injecting Non-Medical Grade Silicone Into The Bodies Of Victim Customers

FDA - U.S. Food and Drug Administration

22-9-2017

Criminal and civil actions filed against Aegerion Pharmaceuticals Inc.

Criminal and civil actions filed against Aegerion Pharmaceuticals Inc.

Aegerion Pharmaceuticals Inc. agreed to plead guilty in the United States District Court for the District of Massachusetts to two misdemeanor counts of violating the Federal Food, Drug, and Cosmetic Act (FD&C Act) involving the introduction of misbranded Juxtapid (lomitapide) into interstate commerce.

FDA - U.S. Food and Drug Administration

11-9-2017

 DKMA Update

DKMA Update

Our newsletter Danish Pharmacovigilance Update changes name to DKMA Update and will from now on contain information about medicinal products in general, patient safety and life science. DKMA Update is an electronic newsletter intended for anyone who work with medicines, either clinically or in the pharmaceutical industry or the retail industry, and people who would like to gain an insight into our work. The newsletter will continue to focus on the most recent safety updates, but will also focus on other...

Danish Medicines Agency

19-4-2018

Turn Chores Into a Fitness Routine

Turn Chores Into a Fitness Routine

Title: Turn Chores Into a Fitness RoutineCategory: Health NewsCreated: 4/18/2018 12:00:00 AMLast Editorial Review: 4/18/2018 12:00:00 AM

US - MedicineNet

6-4-2018

Here's How to Pack Protein Into Your Diet

Here's How to Pack Protein Into Your Diet

Title: Here's How to Pack Protein Into Your DietCategory: Health NewsCreated: 4/5/2018 12:00:00 AMLast Editorial Review: 4/5/2018 12:00:00 AM

US - MedicineNet

15-3-2018

Jobs That Keep the Mind Sharp &hellip; Even Into Retirement

Jobs That Keep the Mind Sharp &hellip; Even Into Retirement

Title: Jobs That Keep the Mind Sharp … Even Into RetirementCategory: Health NewsCreated: 3/14/2018 12:00:00 AMLast Editorial Review: 3/14/2018 12:00:00 AM

US - MedicineNet

13-3-2018

Early Periods Tied to Mental Health Issues Into Adulthood

Early Periods Tied to Mental Health Issues Into Adulthood

Title: Early Periods Tied to Mental Health Issues Into AdulthoodCategory: Health NewsCreated: 3/9/2018 12:00:00 AMLast Editorial Review: 3/12/2018 12:00:00 AM

US - MedicineNet

2-3-2018

Eyes May Be Window Into Future Memory Loss

Eyes May Be Window Into Future Memory Loss

Title: Eyes May Be Window Into Future Memory LossCategory: Health NewsCreated: 2/28/2018 12:00:00 AMLast Editorial Review: 3/1/2018 12:00:00 AM

US - MedicineNet

23-2-2018

More Americans Pushed Into High-Deductible Health Plans

More Americans Pushed Into High-Deductible Health Plans

Title: More Americans Pushed Into High-Deductible Health PlansCategory: Health NewsCreated: 2/22/2018 12:00:00 AMLast Editorial Review: 2/22/2018 12:00:00 AM

US - MedicineNet

7-2-2018

Upcoming changes to the Permissible Ingredients Determination

Upcoming changes to the Permissible Ingredients Determination

Proposed changes intended to be incorporated into the Permissible Ingredients Determination for March 2018 and June 2018.

Therapeutic Goods Administration - Australia

25-1-2018

Turn Your Commute Into a Daily Workout

Turn Your Commute Into a Daily Workout

Title: Turn Your Commute Into a Daily WorkoutCategory: Health NewsCreated: 1/24/2018 12:00:00 AMLast Editorial Review: 1/24/2018 12:00:00 AM

US - MedicineNet

22-1-2018

Potassium Iodide

Potassium Iodide

Potassium iodide is a thyroid blocker indicated to help prevent radioactive iodine from getting into the thyroid gland during a nuclear radiation emergency.

US - RxList

19-1-2018

Packets That Turn Opioid Painkillers Into Useless Gel Offered at Walmart

Packets That Turn Opioid Painkillers Into Useless Gel Offered at Walmart

Title: Packets That Turn Opioid Painkillers Into Useless Gel Offered at WalmartCategory: Health NewsCreated: 1/18/2018 12:00:00 AMLast Editorial Review: 1/18/2018 12:00:00 AM

US - MedicineNet

10-1-2018

Scientists Turn Skin Cells Into Muscle Cells, a Potential Boon for Research

Scientists Turn Skin Cells Into Muscle Cells, a Potential Boon for Research

Title: Scientists Turn Skin Cells Into Muscle Cells, a Potential Boon for ResearchCategory: Health NewsCreated: 1/9/2018 12:00:00 AMLast Editorial Review: 1/9/2018 12:00:00 AM

US - MedicineNet

16-12-2017

Insights Into Pain Relief From the Family That Can't Feel Pain

Insights Into Pain Relief From the Family That Can't Feel Pain

Title: Insights Into Pain Relief From the Family That Can't Feel PainCategory: Health NewsCreated: 12/14/2017 12:00:00 AMLast Editorial Review: 12/15/2017 12:00:00 AM

US - MedicineNet

14-12-2017

EU/3/17/1952 (PhaseRx Ireland, Ltd)

EU/3/17/1952 (PhaseRx Ireland, Ltd)

EU/3/17/1952 (Active substance: Modified messenger ribonucleic acid encoding human argininosuccinate lyase enzyme encapsulated into lipid nanoparticles) - Orphan designation - Commission Decision (2017)8784 of Thu, 14 Dec 2017 European Medicines Agency (EMA) procedure number: EMA/OD/153/17

Europe -DG Health and Food Safety

28-11-2017

Australian State &amp; Territory variations from Part 4 of the Poisons Standard

Australian State &amp; Territory variations from Part 4 of the Poisons Standard

Part 4 of The Poisons Standard is a record of decisions regarding the classification of medicines and chemicals into Schedules. States and territories can refer to the Poisons Standard as published or enact state or territory variations to the Poisons...

Therapeutic Goods Administration - Australia

8-11-2017

Divers May Be Plunging Into Trouble

Divers May Be Plunging Into Trouble

Title: Divers May Be Plunging Into TroubleCategory: Health NewsCreated: 11/7/2017 12:00:00 AMLast Editorial Review: 11/8/2017 12:00:00 AM

US - MedicineNet

31-10-2017

RAGWITEK (Ambrosia Artemisiifolia Pollen) Tablet [ALK-Abell A/S]

RAGWITEK (Ambrosia Artemisiifolia Pollen) Tablet [ALK-Abell A/S]

Updated Date: Oct 31, 2017 EST

US - DailyMed

31-10-2017

GRASTEK (Timothy Grass Pollen Allergen Extract) Tablet [ALK-Abell A/S]

GRASTEK (Timothy Grass Pollen Allergen Extract) Tablet [ALK-Abell A/S]

Updated Date: Oct 31, 2017 EST

US - DailyMed

20-10-2017

Baclofen vs. Flexeril

Baclofen vs. Flexeril

Baclofen and Flexeril (cyclobenzaprine) are muscle relaxants used f as an adjunct to rest and physical therapy for relief of muscle spasm associated with acute, painful musculoskeletal conditions. Baclofen is also used to treat muscle clonus, rigidity, and pain caused by multiple sclerosis. Baclofen is also injected into the spinal cord to treat severe spasticity from , spinal cord injuries, and other spinal cord diseases.

US - RxList

17-10-2017

News and press releases:  EMA’s procedural handling of safety review was complete and independent

News and press releases: EMA’s procedural handling of safety review was complete and independent

European Ombudsman concludes her inquiry into the HPV vaccines referral

Europe - EMA - European Medicines Agency

6-10-2017

FDA OKs First Test to Screen Zika Virus in Donated Blood

FDA OKs First Test to Screen Zika Virus in Donated Blood

A test for screening donated blood for the Zika virus that was pressed into service on an experimental basis during last year's red-alert outbreak was approved today by the US Food and Drug Administration (FDA).

US - RxList

26-9-2017

Liquid Biopsy May Identify Lung Cancer Tx Failures

Liquid Biopsy May Identify Lung Cancer Tx Failures

SAN DIEGO — The blood-based biomarker of circulating tumor DNA (ctDNA) may catapult the management of nonmetastatic lung cancer into the age of precision medicine, suggest new study results presented here at the American Society for Radiation Oncology (ASTRO) 2017 Annual Meeting.

US - RxList

12-9-2017

Outcomes of advertising complaints - compliance following TGA intervention

Outcomes of advertising complaints - compliance following TGA intervention

Commencement of the publication of outcomes of TGA investigations into advertising complaints

Therapeutic Goods Administration - Australia