AFIA ALCOHOL-FREE FOAMING HAND SANITIZER- benzalkonium chloride solution
National Chemical Laboratories, Inc.

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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Listing of Alcohol-Free Foaming Hand Sanitizer in multiple packages

Drug Facts

Active Ingredient. Purpose

Benzalkonium Chloride 0.13%....... 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 a doctor if irritation or redness develops, or if condition persist 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, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Fragrance, Glyceth-17 Cocoate, Citric Acid

Uses

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

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

Afia Alcohol-Free Foaming Hand Sanitizer

Afia Alcohol-Free Hand Sanitizer

AFIA ALCOHOL-FREE FOAMING HAND SANITIZER
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71023-045
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg in 1 mL

Ingredient Name	Strength
Inactive Ingredients
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)
GLYCERETH-17 COCOATE (UNII: 3057VPT0KC)
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date
Packaging
1	NDC:71023-045-57	1000 mL in 1 BAG; Type 0: Not a Combination Product	05/08/2023
2	NDC:71023-045-29	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/08/2023
3	NDC:71023-045-32	208175 mL in 1 DRUM; Type 0: Not a Combination Product	05/08/2023

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph not final	part333A	05/01/2023

Labeler - National Chemical Laboratories, Inc. (002289619)

Name	Address	ID/FEI	Business Operations
Establishment
National Chemical Laboratories, Inc.		002289619	manufacture(71023-045)