Afia Alcohol-Free Foaming Hand Sanitizer

Dosage form: soap
Ingredients: BENZALKONIUM CHLORIDE 1mg in 1mL
Labeler: National Chemical Laboratories, Inc.
NDC code: 71023-445

Medically reviewed by Drugs.com. Last updated on Mar 10, 2025.

Listing of Alcohol-Free Foaming Hand Sanitizer in multiple packages

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. If swallowed, get medical help or contact a Poison Control Center right away.

Afia Alcohol-Free Foaming Hand Sanitizer

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	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (BENZALKONIUM)	BENZALKONIUM CHLORIDE	1 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERETH-2 COCOATE
BEHENTRIMONIUM CHLORIDE
DIHYDROXYETHYL COCAMINE OXIDE
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE
WATER

Packaging
#	Item Code	Package Description
1	NDC:71023-445-57	1000 mL in 1 BAG
2	NDC:71023-445-29	3785 mL in 1 BOTTLE, PLASTIC
3	NDC:71023-445-32	208450 mL in 1 DRUM

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	Operations
National Chemical Laboratories, Inc.		002289619	manufacture(71023-445)

Revised: 03/2020

Document Id: a14bb7ec-8ebe-0ef2-e053-2995a90a59e9

Set id: 3e85ad4a-59bf-4629-e054-00144ff8d46c

Version: 7

Effective Time: 20200320

National Chemical Laboratories, Inc.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer

Afia Alcohol-Free Foaming Hand Sanitizer

Further information

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Zepbound

Wegovy

Victoza

Saxenda

Alli

Methamphetamine

Amphetamine

Tirzepatide