Amerfresh Antibacterial Deodorant

Manufacturer: Liufangjing Biotechnology (Yangzhou) Co., Ltd
Effective date: 2025-09-09
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:13:20

Label at a glance#

ProductAmerfresh Antibacterial Deodorant

Active ingredientBENZETHONIUM CHLORIDE

Label structure9 sections

Dosage and administration

Wet bar with water Lather vigorously and wash skin Rinse and dry thoroughly

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride 0.1%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

For washing to decrease bacteria on skin

Warnings

WARNINGS SECTION

For external use only

Do not use this product on infants under 6

OTC - WHEN USING SECTION

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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Wet bar with water

Lather vigorously and wash skin

Rinse and dry thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1872091	benzethonium chloride 0.1 % Medicated Bar Soap	PSN	2
1872091	benzethonium chloride 0.001 MG/MG Medicated Bar Soap	SCD	2
1872091	benzethonium chloride 0.1 % Medicated Bar Soap	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
85420-002-01	Amerfresh Antibacterial Deodorant	10 g in 1 APPLICATOR	SOAP	10	2
85420-002-01	Amerfresh Antibacterial Deodorant	1 in 1 PACKAGE	SOAP	1	2
85420-002-02	Amerfresh Antibacterial Deodorant	1 in 1 PACKAGE	SOAP	1	2
85420-002-02	Amerfresh Antibacterial Deodorant	36 g in 1 APPLICATOR	SOAP	36	2
85420-002-03	Amerfresh Antibacterial Deodorant	1 in 1 PACKAGE	SOAP	1	2
85420-002-03	Amerfresh Antibacterial Deodorant	68 g in 1 APPLICATOR	SOAP	68	2
85420-002-04	Amerfresh Antibacterial Deodorant	85 g in 1 APPLICATOR	SOAP	85	2
85420-002-04	Amerfresh Antibacterial Deodorant	1 in 1 PACKAGE	SOAP	1	2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

Amerfresh Antibacterial Deodorant
BENZETHONIUM CHLORIDE
WATER
SODIUM PALM KERNELATE
PALM ACID
SODIUM PALMATE
SODIUM CHLORIDE
GLYCERIN
COCONUT ACID
EDETATE SODIUM
CITRIC ACID MONOHYDRATE
SODIUM TALLOWATE
SODIUM COCOATE
BENZETHONIUM

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
85420-002	85420-002-01, 85420-002-02, 85420-002-03, 85420-002-04

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
SODIUM PALM KERNELATE	6H91L1NXTW	IACT
PALM ACID	B6G0Y5Z616	IACT
SODIUM PALMATE	S0A6004K3Z	IACT
SODIUM CHLORIDE	451W47IQ8X	IACT
GLYCERIN	PDC6A3C0OX	IACT
COCONUT ACID	40U37V505D	IACT
EDETATE SODIUM	MP1J8420LU	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
SODIUM TALLOWATE	07RIK6QMEW	IACT
SODIUM COCOATE	R1TQH25F4I	IACT
BENZETHONIUM CHLORIDE	PH41D05744	ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Amerfresh Antibacterial Deodorant	BENZETHONIUM CHLORIDE	Liufangjing Biotechnology (Yangzhou) Co., Ltd	cdc4f0ff-07bd-47c8-850b-1698308bb660	2025-09-09	Warnings	Exact identifier ndc (package): 85420-002-04 ndc (package): 85420-002-01 ndc (package): 85420-002-02 ndc (package): 85420-002-03 ndc (product): 85420-002 ndc11 (package): 85420000203 ndc11 (package): 85420000201 ndc11 (package): 85420000204 ndc11 (package): 85420000202 spl id: 3e602541-757a-9f8a-e063-6394a90aeaaa spl set id: cdc4f0ff-07bd-47c8-850b-1698308bb660

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.