ANTI BACTERIAL HAND SANITIZER- ethyl alcohol gel

Nazione: Stati Uniti

Lingua: inglese

Fonte: NLM (National Library of Medicine)

Compra

Scheda tecnica Scheda tecnica (SPC)
21-02-2016

Principio attivo:

ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Commercializzato da:

Dolgencorp Inc.

INN (Nome Internazionale):

ALCOHOL

Composizione:

ALCOHOL 62 mL in 100 mL

Via di somministrazione:

TOPICAL

Tipo di ricetta:

OTC DRUG

Indicazioni terapeutiche:

Purpose: Antiseptic Stop use or ask for a doctor if redness or irritation develops and persists for more than 72 hours. Uses: Hand sanitizer to help decrease bacteria on the skin when water, soap & towel are not available. Recommended for repeated use.

Stato dell'autorizzazione:

OTC monograph not final

Scheda tecnica

                                ANTI BACTERIAL HAND SANITIZER- ETHYL ALCOHOL GEL
DOLGENCORP INC.
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
----------
ACTIVE INGREDIENTS:
Ethyl Alcohol 62%
PURPOSE:
Antiseptic
WARNINGS: For external use only.
Flammable. Keep away from fire or flame.
Do not apply around eyes.
Do not use in ears or mouth.
When using this product, avoid contact with eyes. In case of contact,
flush eyes with water.
Stop use or ask for a doctor if redness or irritation develops and
persists for more than 72 hours.
Keep out of reach of children. Children must be supervised in use of
this product.
DIRECTIONS:
Pump as needed into your palms and thoroughly spread on both hands.
Rub into skin until dry.
INACTIVE INGREDIENTS: Water, Glycerin, Propylene Glycol, Carbomer,
Triethanolamine, Aloe
Barbadenis Leaf Juice
OTHER INFORMATION: Do not store in temperature over 118 F.
USES: Hand sanitizer to help decrease bacteria on the skin when water,
soap & towel are not available.
Recommended for repeated use.
ANTI BACTERIAL HAND SANITIZER
ethyl alcohol gel
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:559 10 -9 8 8
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
6 2 mL in 10 0 mL
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
ALO E VERA LEAF (UNII: ZY8 1Z8 3H0 X)
Dolgencorp Inc.
GLYCERIN (UNII: PDC6 A3C0 OX)
PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3)
CARBO MER INTERPO LYMER TYPE A ( 550 0 0 CPS) (UNII: 59 TL3WG5CO)
TRO LAMINE (UNII: 9 O3K9 3S3TK)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START
DATE
MARKETING END
DATE
1
NDC:559 10 -9 8 8 -
47
29 mL in 1 BOTTLE, SPRAY; Type 0 : No t a Co mbinatio n
Pro duc t
0 2/22/20 16
MARKETING INFORMATION
MARKE TING CATE GORY
APPLICATION NUMBE R OR MO
                                
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