AFIA ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride soap

Afia Alcohol-Free Foaming Hand Sanitizer by

Drug Labeling and Warnings

Afia Alcohol-Free Foaming Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by National Chemical Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient. Purpose

Benzalkonium Chloride 0.1%...........Antimicrobial

Uses

• For hand sanitizing to decrease bacteria on the skin
• Recommended for repeated use

Warnings:

For external use only.

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask doctor if irritation or redness developts, or if condition persists for more than 72 hours.

Directions

• Pump a small amount of foam into palm of hand
• Rub thoroughly over all surfaces of both hands
• Rub hands together briskly until dry

Inactive ingredients

Water, dihyroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

Uses

For hand sanitizing to decrease bacteria on the skin
Recommended for repeated use

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.

PRINCIPAL DISPLAY PANEL

Afia Alcohol-Free Foaming Hand Sanitizer

INGREDIENTS AND APPEARANCE

AFIA ALCOHOL-FREE FOAMING HAND SANITIZER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71023-445
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)
BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE (UNII: 0Y0NQR2GH1)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71023-445-57	1000 mL in 1 BAG; Type 0: Not a Combination Product	10/24/2016
2	NDC: 71023-445-29	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2020
3	NDC: 71023-445-32	208450 mL in 1 DRUM; Type 0: Not a Combination Product	03/08/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/24/2016

Labeler - National Chemical Laboratories, Inc. (002289619)

Registrant - National Chemical Laboratories, Inc. (002289619)

Establishment
Name	Address	ID/FEI	Business Operations
National Chemical Laboratories, Inc.		002289619	manufacture(71023-445)