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 FOAMING ANTI-BACTERIAL HAND CLEANER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71023-046
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
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 Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71023-046-57	1000 mL in 1 BAG; Type 0: Not a Combination Product	05/08/2023	05/06/2024
2	NDC: 71023-046-29	3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/08/2023	05/06/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	05/08/2023	05/06/2024

Labeler - National Chemical Laboratories, Inc. (002289619)

Registrant - National Chemical Laboratories, Inc. (002289619)

Establishment
Name	Address	ID/FEI	Business Operations
National Chemical Laboratories, Inc.		002289619	manufacture(71023-046)

Revised: 7/2024

Document Id: 1c5985ea-746c-a5d6-e063-6294a90ac04a

34390-5

Set id: fa1c1c15-c9a5-9d7f-e053-6294a90a9e32

Version: 3

Effective Time: 20240703