AFIA FOAMING ANTI-BACTERIAL HAND CLEANER- benzalkonium chloride soap 
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 Afia Foaming Anti-Bacterial Hand Cleaner

Drug Facts

Active Ingredient. Purpose

Benzalkonium Chloride 0.13%............Antimicrobial

USE

For hand washing to decrease bacteria on the skin

Uses

For hand washing to decrease bacteria on the skin

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 persists for more than 72 hours.

Directions

Inactive ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Cocamidopropyl PG-Dimonium Chloride Phosphate, Glycereth-2 Cocoate, Phenoxyethanol, Cocamidopropyl Hydroxysultaine, fragrance, Benzoic Acid, Methylisothiazolinone, FD&C yellow 5, FD&C blue 1

Warnings:

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

Afia Anti-Bacterial Foaming Hand Cleaner

Afia Anti-Bacterial Foaming Hand Cleaner labelAfia Anti-Bacterial Foaming Hand Cleaner

AFIA FOAMING ANTI-BACTERIAL HAND CLEANER 
benzalkonium chloride soap
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71023-046
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
LAURTRIMONIUM CHLORIDE (UNII: A81MSI0FIC)  
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
DIHYDROXYETHYL COCAMINE OXIDE (UNII: 8AR51R3BL5)  
COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: H2KVQ74JM4)  
GLYCERETH-2 COCOATE (UNII: JWM00VS7HC)  
WATER (UNII: 059QF0KO0R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)  
BENZOIC ACID (UNII: 8SKN0B0MIM)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71023-046-571000 mL in 1 BAG; Type 0: Not a Combination Product05/08/2023
2NDC:71023-046-293785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/08/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A05/08/2023
Labeler - National Chemical Laboratories, Inc. (002289619)
Registrant - National Chemical Laboratories, Inc. (002289619)
Establishment
NameAddressID/FEIBusiness Operations
National Chemical Laboratories, Inc.002289619manufacture(71023-046)

Revised: 5/2023
Document Id: fa1c1c15-c9a6-9d7f-e053-6294a90a9e32
Set id: fa1c1c15-c9a5-9d7f-e053-6294a90a9e32
Version: 1
Effective Time: 20230508
 
National Chemical Laboratories, Inc.