Clarifying Face and Body Wash

Manufacturer: Acneology Treatment Center, LLC
Effective date: 2021-09-24
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:42:29

Label at a glance#

ProductClarifying Face and Body Wash

Active ingredientBENZOYL PEROXIDE

Label structure8 sections

Indications and uses

Adults and children 12 years and over: For the treatment of acne For acne-prone or oily skin

Dosage and administration

Use 1 to 3 times daily on affected skin, work into lather, rinse off thoroughly.

Contacts and useful links#

PhoneLabel contact800-439-4166

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl Peroxide 2.5%

Purpose

OTC - PURPOSE SECTION

For the treatment of acne

Uses

INDICATIONS & USAGE SECTION

Adults and children 12 years and over:

For the treatment of acne
For acne-prone or oily skin

Warnings

WARNINGS SECTION

For external use only. Avoid contact with eyes and eyelids. This product may cause irritation. Mild irritation may be reduced by using the product less frequently. If irritation becomes severe, discontinue use and consult a doctor.

Do not use

OTC - DO NOT USE SECTION

this product if you have very sensitive skin or if you are sensitive to benzoyl peroxide.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contacting Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Use 1 to 3 times daily on affected skin, work into lather, rinse off thoroughly.

Other Information

SPL UNCLASSIFIED SECTION

May bleach hair or fabrics.
Store at room temperature.
Keep away from heat or direct sunlight.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Ammonium Lauryl Sulfate, Glycerin, Disodium Cocoamphodiacetate, Propylene Glycol, Carbomer, Sodium Hydroxide.

Questions or Comments?

OTC - QUESTIONS SECTION

Call Toll-Free 800-439-4166

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
845836	benzoyl peroxide 2.5 % Medicated Liquid Soap	PSN	4
845836	benzoyl peroxide 25 MG/ML Medicated Liquid Soap	SCD	4
845836	benzoyl peroxide 2.5 % Medicated Liquid Soap	SY	4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
a46239a7-5963-4008-8cbb-6b9000f497eb	Product name	1	20250721
b382b4e1-6b48-45f6-bffc-e61b00b0ce19	Product name	3	20250317
d9d61457-6a5a-41fc-b418-e5479a2904b7	Product name	2	20230303
32012d5c-25ac-49c7-9d4c-1313177fff7c	Product name	1	20230112
13e7e7e3-e885-4c79-af6d-dad1aedbb06e	Product name	1	20220128
4a7d44fe-774d-404b-aad0-8a90fe78375a	Product name	4	20211025
3f45980c-c196-47e5-0e5e-48b7c57327c5	Product name	5	20200428
d12e2d7c-bd6b-45d4-94f9-6df8e1b8b27b	Product name	3	20200203
ee5c6de5-d9cd-454f-b250-7b19e5cf2992	Product name	4	20190619
ad75fcfd-a339-42a1-9c60-43ba2c654cfa	Product name	1	20170810

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73610-000-00	2023-01-30	C162847	48780-1	f386c64a-2420-0266-e053-dadaa90a7c1a	Clarifying Face & Body Wash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73610-000-00	Clarifying Face and Body Wash	180 mL in 1 BOTTLE	LIQUID	180		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73610-000	CLARIFYING FACE AND BODY WASH (BENZOYL PEROXIDE) LIQUID [ACNEOLOGY TREATMENT CENTER, LLC]	4	Legacy NDC, 1 package rows	20210925_3083f963-8e20-4298-9e79-005990414394.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

Clarifying Face and Body Wash
BENZOYL PEROXIDE
WATER
AMMONIUM LAURYL SULFATE
GLYCERIN
DISODIUM COCOAMPHODIACETATE
PROPYLENE GLYCOL
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
SODIUM HYDROXIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73610-000	73610-000-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
AMMONIUM LAURYL SULFATE	Q7AO2R1M0B	IACT
GLYCERIN	PDC6A3C0OX	IACT
DISODIUM COCOAMPHODIACETATE	18L9G3U51M	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE	0A5MM307FC	IACT
SODIUM HYDROXIDE	55X04QC32I	IACT
BENZOYL PEROXIDE	W9WZN9A0GM	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
ccbfb8d8-d066-252c-e053-2995a90aa5bb			3083f963-8e20-4298-9e79-005990414394	2021-09-24	Warnings	Exact identifier spl id: ccbfb8d8-d066-252c-e053-2995a90aa5bb spl set id: 3083f963-8e20-4298-9e79-005990414394

Reported adverse events (FAERS/openFDA)#

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