INSTANT SANITIZING SOFT WIPES- alcohol swab

País: Estados Unidos

Língua: inglês

Origem: NLM (National Library of Medicine)

Ingredientes ativos:

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

Disponível em:

GUANGDONG KINGFA SCI.&TECH.CO.,LTD.

Via de administração:

TOPICAL

Tipo de prescrição:

OTC DRUG

Indicações terapêuticas:

Purpose: Antimicrobial For sanitizing to help reduce bacteria on the skin. in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts.

Status de autorização:

OTC monograph not final

Características técnicas

INSTANT SANITIZING SOFT WIPES- ALCOHOL SWAB
GUANGDONG KINGFA SCI.&TECH.CO.,LTD.
_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._
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75 ALCOHOL JINFA
ACTIVE INGREDIENT(S)
Alcohol 75% v/v.
PURPOS E
Purpose: Antimicrobial
US ES
For sanitizing to help reduce bacteria on the skin.
WARNINGS
Flammable.Keep away from fire or flame. For external use only.
When using this product, avoid contact with eyes.
DO NOT USE
in or near the eyes. In case of contact, rinse eyes thoroughly with
water.
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep out of reach of children. If swallowed, get medical help or
contact a Poison Control Center right
away.
DIRECTIONS
Rub thoroughly over all surfaces of both hands with wipe. Allow to dry
without wiping.
Keep away from dirct sunlight; store in a cool, dry place.
OTHER INFORMATION
Store below 104F(40C)
May discolor certain fabrics.
Don't put it in the car, keep away from high temperature.
INACTIVE INGREDIENTS
Water(Aqua)
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
1 PCS NDC 80974-001-01
20PCS NDC 80974-001-02
50PCS NDC 80974-001-03
80PCS NDC 80974-001-04
60PCS NDC 80974-001-05
100PCS NDC 80974-001-06
160PCS NDC 80974-001-07
INSTANT SANITIZING SOFT WIPES
alcohol swab
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:8 0 9 74-0 0 1
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
75 g in 10 0 g
INACTIVE INGREDIENTS
INGREDIENT NAME
STRE NG TH
WATER (UNII: 0 59 QF0 KO0 R)
PACKAG ING
#
ITEM CODE
PACKAGE DESCRIPTION
MARKETING START DATE
MARKETING END DATE
1
NDC:8 0 9 74-0 0 1-0 1
1 in 1 BAG
12/15/20 20
GUANGDONG KINGFA SCI.&TECH.CO.,LTD.
1
5 g in 1 APPLICATOR; Type 0 : No t a Co mbinatio n Pro duct
2
NDC:8 0 9 74-0 0 1-0 2
20 in 1 BAG
12/15/20 20
2
5 g in 1 AP