Amazon Commercial Antibacterial Foaming Skin Cleanser

Amazon Commercial Antibacterial Foaming Skin Cleanser by

Drug Labeling and Warnings

Amazon Commercial Antibacterial Foaming Skin Cleanser by is a Otc medication manufactured, distributed, or labeled by Amazon, Betco Corporation, Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

AMAZON COMMERCIAL ANTIBACTERIAL FOAMING SKIN CLEANSER- benzalkonium chloride soap 
Amazon

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Amazon Commercial Antibacterial Foaming Skin Cleanser

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Warnings

• For external use only. Do not ingest.
• Avoid contact with eyes.  If contact occurs, rinse thoroughly with water.
• Stop use and ask a doctor if irritation and redness develop.
• If irritation persists for more than 72 hours, consult a physician.
• KEEP OUT OF REACH OF CHILDREN.
• If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• ?Read the entire label before using this product.
• ?Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands.
• Rinse with clean water.

Inactive Ingredients

Water, Lauramine Oxide, Decyl Glucoside, Propylene Glycol, PEG-4 Rapeseedamine, Cocamidopropyl Hydroxysultaine, Glycerin, Fragrance, Tetrasodium EDTA, Citric Acid, Methylchloroisothiazolinone, Methylisosthiazolinone, FD&C Blue #1.

Questions? 888-GO BETCO (888-462-3826)

Amazon Commerical Antibacterial Foam

Purpose

Antibacterial

Amazon Commerical Antibacterial Foam

KEEP OUT OF REACH OF CHILDREN

Amazon Commerical Antibacterial Foam

AMAZON COMMERCIAL ANTIBACTERIAL FOAMING SKIN CLEANSER 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72288-759
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
WATER (UNII: 059QF0KO0R)
COCAMINE OXIDE (UNII: QWA2IZI6FI)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PEG-4 RAPESEEDAMIDE (UNII: 89575CN928)
COCAMIDOPROPYL HYDROXYSULTAINE (UNII: 62V75NI93W)
GLYCERIN (UNII: PDC6A3C0OX)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE SODIUM (UNII: MP1J8420LU)
ALCOHOL (UNII: 3K9958V90M)
BENZYL ACETATE (UNII: 0ECG3V79ZJ)
SODIUM GLYCOLATE (UNII: B75E535IMI)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
TRISODIUM NITRILOTRIACETATE (UNII: E3C8R2M0XD)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
N-ALKYL DIMETHYL BENZYL AMMONIUM CHLORIDE (C12-C18) (UNII: 9U1Q4T4ZYS)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
2,4-DIMETHYL-3-CYCLOHEXENE CARBOXALDEHYDE (UNII: 452GFV2AFS)
METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)
CAPRYLYL/CAPRYL OLIGOGLUCOSIDE (UNII: E00JL9G9K0)
MAGNESIUM NITRATE (UNII: 77CBG3UN78)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
GERANIOL (UNII: L837108USY)
LIME OIL (UNII: UZH29XGA8G)
2-METHYLUNDECANAL (UNII: S94QNS2VY5)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
ALLYL CYCLOHEXANEPROPIONATE (UNII: H4W9H3L241)
GERANYL ACETATE (UNII: 3W81YG7P9R)
CITRONELLYL ACETATE (UNII: IZ420RT3OY)
LINALOOL, (+/-)- (UNII: D81QY6I88E)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
CITRAL (UNII: T7EU0O9VPP)
FORMALDEHYDE (UNII: 1HG84L3525)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72288-759-04	3780 mL in 1 JUG; Type 0: Not a Combination Product	11/12/2012

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	11/12/2012	11/20/2024

Labeler - Amazon (128990418)

Registrant - Betco Corporation, Ltd (024492831)

Establishment
Name	Address	ID/FEI	Business Operations
Betco Corporation, Ltd		024492831	manufacture(72288-759) , label(72288-759)

Revised: 11/2024

Document Id: 275b3685-a4ec-94a9-e063-6394a90a20e9

34390-5

Set id: abbfb2f5-67bb-ea94-e053-2995a90ac169

Version: 4

Effective Time: 20241120