Skip to main content

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 11, 2024.

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:71023-445
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (BENZALKONIUM) BENZALKONIUM CHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERETH-2 COCOATE 
BEHENTRIMONIUM CHLORIDE 
DIHYDROXYETHYL COCAMINE OXIDE 
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:71023-445-571000 mL in 1 BAG
2NDC:71023-445-293785 mL in 1 BOTTLE, PLASTIC
3NDC:71023-445-32208450 mL in 1 DRUM
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A10/24/2016
Labeler - National Chemical Laboratories, Inc. (002289619)
Registrant - National Chemical Laboratories, Inc. (002289619)
Establishment
NameAddressID/FEIOperations
National Chemical Laboratories, Inc.002289619manufacture(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