ANTISEPTIC WIPE- benzalkonium chloride swab

ANTISEPTIC WIPE by

Drug Labeling and Warnings

ANTISEPTIC WIPE by is a Otc medication manufactured, distributed, or labeled by Guangdong Comfort Medical Products Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium chloride 0.13%

PURPOSE

First Aid Antiseptic

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.

INDICATIONS & USAGE

Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water.

WARNINGS

For external use only.

DOSAGE & ADMINISTRATION

Tear open packet, unfold and use as a washcloth. Allow hands to dry without wiping.

INACTIVE INGREDIENT

Water

PRINCIPAL DISPLAY PANEL

ACTIVE INGREDIENT:
Benzalkonium chloride 0.13%
PURPOSE:
First Aid Antiseptic
USES:
Antiseptic cleansing of face, hands and body to decrease bacteria on skin without soap and water.
WARNINGS:
For external use only.
DO NOT USE:
in the eyes. Ifthis happens, rinse thoroughly with water.
STOP USE and ASK A DOCTOR:
If irritation or redness develop and persists for more than 72 hours.
CAUTION:
Keep out of reach of children, If swallowed, get medical help or contact a Poison Control Center right away.
DIRECTIONS:
Tear open packet, unfold and use as a washcloth. Allow hands to dry without wiping.
OTHER INFORMATION:
Store at room temperature.
INACTIVE INGREDIENTS:
water

INGREDIENTS AND APPEARANCE

ANTISEPTIC WIPE 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71584-0002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71584-0002-1	1.6 g in 1 PACKET; Type 0: Not a Combination Product	09/15/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	09/15/2022

Labeler - Guangdong Comfort Medical Products Co., Ltd. (544507534)

Registrant - Guangdong Comfort Medical Products Co., Ltd. (544507534)