ALCOHOL ANTIBACTERIAL WIPES cloth

Pajjiż: Stati Uniti

Lingwa: Ingliż

Sors: NLM (National Library of Medicine)

Ixtrih issa

Ingredjent attiv:

CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y) (CHLORHEXIDINE - UNII:R4KO0DY52L), BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y), ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)

Disponibbli minn:

Kunming Ansheng Industry & Trade Co., Ltd.

Rotta amministrattiva:

TOPICAL

Tip ta 'preskrizzjoni:

OTC DRUG

Indikazzjonijiet terapewtiċi:

Antibacterial Hand Sanitizer to reduce bacteria on the skin - in children less than 2 months of age - on open skin wounds Stop use and ask a doctor if irritation or rash appears and lasts

L-istatus ta 'awtorizzazzjoni:

OTC monograph not final

Karatteristiċi tal-prodott

                                ALCOHOL ANTIBACTERIAL WIPES- ALCOHOL ANTIBACTERIAL WIPES CLOTH
KUNMING ANSHENG INDUSTRY & TRADE 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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ALCOHOL ANTIBACTERIAL WIPES
ACTIVE INGREDIENT(S)
ethanol15.0%
Chlorhexidine diacetate0.1%
Benzalkonium chloride0.1%
PURPOS E
Antibacterial
US E
Hand Sanitizer to reduce bacteria on the skin
WARNINGS
Flammable. Keep away from heat or flame
do not use in or contact the eyes or damaged skin
DO NOT USE
in children less than 2 months of age
on open skin wounds
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
peel the sticker when you use it. Easily get one wipe at a time. After
application, please re-seal the
opening sticker firmly to prevent wipes from drying out
INACTIVE INGREDIENTS
pure water
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
ALCOHOL ANTIBACTERIAL WIPES
alcohol antibacterial wipes cloth
Kunming Ansheng Industry & Trade Co., Ltd.
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:78 18 3-0 15
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
CHLO RHEXIDINE ACETATE (UNII: 59 0 8 ZUF22Y) (CHLORHEXIDINE -
UNII:R4KO0 DY52L)
CHLORHEXIDINE
ACETATE
0 .1 g
in 10 0 a
BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6 JUD5X6 Y)
BENZALKONIUM
CHLORIDE
0 .1 g
in 10 0 a
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
15 g in 10 0 a
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:78 18 3-0 15-0 1
50 a in 1 BAG; Type 0 : No t a Co mbinatio n Pro duct
0 3/30 /20 20
2
NDC:78 18 3-0 15-0 2
8 0 a in 1 BAG; Type 0 : No t a Co mbinatio n P
                                
                                Aqra d-dokument sħiħ