Listing of Afia Foaming Anti-Bacterial Hand Cleaner

Afia Foaming Anti-Bacterial Hand Cleaner by

Drug Labeling and Warnings

Afia Foaming Anti-Bacterial Hand Cleaner by is a Otc medication manufactured, distributed, or labeled by National Chemical Laboratories, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AFIA FOAMING ANTI-BACTERIAL HAND CLEANER- benzalkonium chloride soap 
National Chemical Laboratories, Inc.

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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

  • Wet a hand. Pump one or two stokes of foam, into palm of hand.
  • Rub thoroughly over all surfacesof both hands for 30 seconds
  • Rinse hands and dry thoroughly.

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 Product05/08/202305/06/2024
2NDC: 71023-046-293785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/08/202305/06/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01405/08/202305/06/2024
Labeler - National Chemical Laboratories, Inc. (002289619)
Registrant - National Chemical Laboratories, Inc. (002289619)
Establishment
NameAddressID/FEIBusiness Operations
National Chemical Laboratories, Inc.002289619manufacture(71023-046)

Revised: 7/2024