Listing of Alcohol-Free Foaming Hand Sanitizer in multiple packages

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]

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

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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 TypeHUMAN OTC DRUGItem Code (Source)NDC: 71023-045
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 71023-045-571000 mL in 1 BAG; Type 0: Not a Combination Product05/08/202305/06/2024
2NDC: 71023-045-293785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/08/202305/06/2024
3NDC: 71023-045-32208175 mL in 1 DRUM; Type 0: Not a Combination Product05/08/202305/06/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01405/01/202305/06/2024
Labeler - National Chemical Laboratories, Inc. (002289619)
Establishment
NameAddressID/FEIBusiness Operations
National Chemical Laboratories, Inc.002289619manufacture(71023-045)

Revised: 7/2024
Document Id: 1c5988b4-16d5-be18-e063-6294a90ad3d5
Set id: fa690ebf-a7ae-558f-e053-6294a90a3c75
Version: 3
Effective Time: 20240703