AMERFRESH ANTIBACTERIAL DEODORANT- benzethonium chloride soap

Amerfresh Antibacterial Deodorant by

Drug Labeling and Warnings

Amerfresh Antibacterial Deodorant by is a Otc medication manufactured, distributed, or labeled by Liufangjing Biotechnology (Yangzhou) Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzethonium Chloride 0.1%

Purpose

Antibacterial

Use

For washing to decrease bacteria on skin

Warnings

For external use only

Do not use this product on infants under 6

WHEN USING

When using this product avoid contact with eyes. In case of eye contact flush with water

KEEP OUT OF REACH OF CHILDREN

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

Directions

Wet bar with water

Lather vigorously and wash skin

Rinse and dry thoroughly

Inactive ingredients

Soap (Sodium Palmate and/or Sodium Tallowate, Sodium Cocoate and/or Sodium Palm Kernelate),  Water, Palm Acid, Glycerin, Coconut Acid, Fragrance, tetrasodium EDTA, Citric Acid Anhydrous

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

AMERFRESH ANTIBACTERIAL DEODORANT 
benzethonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85420-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM PALMATE (UNII: S0A6004K3Z)
WATER (UNII: 059QF0KO0R)
SODIUM PALM KERNELATE (UNII: 6H91L1NXTW)
PALM ACID (UNII: B6G0Y5Z616)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
GLYCERIN (UNII: PDC6A3C0OX)
COCONUT ACID (UNII: 40U37V505D)
EDETATE SODIUM (UNII: MP1J8420LU)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM TALLOWATE (UNII: 07RIK6QMEW)
SODIUM COCOATE (UNII: R1TQH25F4I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85420-002-01	1 in 1 PACKAGE	05/20/2027
1		10 g in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 85420-002-02	1 in 1 PACKAGE	05/20/2027
2		36 g in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 85420-002-03	1 in 1 PACKAGE	05/20/2027
3		68 g in 1 APPLICATOR; Type 0: Not a Combination Product
4	NDC: 85420-002-04	1 in 1 PACKAGE	05/20/2027
4		85 g in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	05/20/2025

Labeler - Liufangjing Biotechnology (Yangzhou) Co., Ltd (510194010)

Establishment
Name	Address	ID/FEI	Business Operations
Liufangjing Biotechnology (Yangzhou) Co., Ltd		510194010	manufacture(85420-002)