NOBLE 75% ALCOHOL WIPES- 75% alcohol wipes cloth

Kraj: Stany Zjednoczone

Język: angielski

Źródło: NLM (National Library of Medicine)

Składnik aktywny:

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

Dostępny od:

Kunming Ansheng Industry & Trade Co., Ltd.

Droga podania:

TOPICAL

Typ recepty:

OTC DRUG

Wskazania:

Antibacterial; kill 99.99% of most common germs. Hand sanitizer to help reduce bacterial 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.

Status autoryzacji:

OTC monograph not final

Charakterystyka produktu

NOBLE 75% ALCOHOL WIPES- 75% ALCOHOL 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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NOBLE 75% ALCOHOL WIPES
ACTIVE INGREDIENT(S)
Alcohol 75% v/v.
Chlorhexidine diacetate 0.1% v/v.
Benzalkonium chloride 0.1% v/v.
PURPOS E
Antibacterial; kill 99.99% of most common germs.
US E
Hand sanitizer to help reduce bacterial on the skin.
WARNINGS
For external use only. Flammable. Keep away from heat or flame
DO NOT USE
in children less than 2 months of age
on open skin wounds
When using this product do not use in or contact the eyes or damaged
skin.
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
Open the sealing sticker when you use it.
You can take it freely.
When not use, please re-tighten the sealing sticker to prevent the
wipes from drying out.
INACTIVE INGREDIENTS
Pure water
PACKAGE LABEL - PRINCIPAL DISPLAY PANEL
50 CLOTH in 1 BAG
NDC: 78183-019-01
NOBLE 75% ALCOHOL WIPES
75% alcohol wipes cloth
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:78 18 3-0 21
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 .0 0 1 U
in 1 U
BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6 JUD5X6 Y)
BENZALKONIUM
CHLORIDE
0 .0 0 1 U
in 1 U
ALCO HO L (UNII: 3K9 9 58 V9 0 M) (ALCOHOL - UNII:3K9 9 58 V9 0 M)
ALCOHOL
0 .75 U in 1 U
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 21-0 1
50 U in 1 BAG; Type 0 : No t a Co mbinatio n Pro duct
12/31/20 20
MARKE