ALCOHOL ANTIBACTERIAL WIPES cloth

Alcohol Antibacterial Wipes by

Drug Labeling and Warnings

Alcohol Antibacterial Wipes by is a Otc medication manufactured, distributed, or labeled by Kunming Ansheng Industry & Trade Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

Alcohol 75% v/v;

Chlorohexidine Diacetate 0.1% v/v;

Benzalkonium 0.1% v/v;

Purpose

Antibacterial

Use

For hand sanitizing to decrease bacterial on the skin.

Warnings

For external use only. Flammable. Keep away from heat or flame

Do not use

• on infants less than 2 months of age
• on open skin wounds

WHEN USING

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

1, Open sticker, pull out the wipe and close sticker tightly.

2, Dispose of used wipes in trash, DO NOT FLUSH.

Other information

Keep in cool dry place, storage temperature: 0-40℃

Inactive ingredients

Inactive ingredients: Water, Chlorohexidine Diacetate, Benzalkonium Chloride

Package Label - Principal Display Panel

30 wipes in one bag. NDC: 78183-018-01

50 wipes in one bag. NDC: 78183-018-02

INGREDIENTS AND APPEARANCE

ALCOHOL ANTIBACTERIAL WIPES 
alcohol antibacterial wipes cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 78183-018
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.75 U  in 1 U

Inactive Ingredients
Ingredient Name	Strength
CHLORHEXIDINE ACETATE (UNII: 5908ZUF22Y)	0.001 U  in 1 U
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)	0.001 U  in 1 U
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 78183-018-01	30 U in 1 BAG; Type 0: Not a Combination Product	06/01/2020
2	NDC: 78183-018-02	50 U in 1 BAG; Type 0: Not a Combination Product	06/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	06/01/2020

Labeler - Kunming Ansheng Industry & Trade Co., Ltd. (421081801)

Establishment
Name	Address	ID/FEI	Business Operations
Kunming Ansheng Industry & Trade Co., Ltd.		421081801	manufacture(78183-018) , label(78183-018)