Acne Cleanser

Manufacturer
Old East Main Co. | Consumer Product Partners, LLC
Effective date
2024-09-23
Label type
HUMAN OTC DRUG LABEL
Version
14
Source
legacy-cache
Hydrated at
2026-08-01 20:54:23

Label at a glance#

ProductAcne Cleanser
Active ingredientBENZOYL PEROXIDE
Label structure13 sections

Dosage and administration

wet face. Gently massage all over face for 20-30 seconds avoiding the eyes.   Rinse thoroughly and pat dry. because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor if bothersome dryness or peeling occurs, reduce daily application to once a day or every other day if going outside, apply sunscreen after...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl peroxide 10%

Purpose

OTC - PURPOSE SECTION

Acne medication

Use

INDICATIONS & USAGE SECTION

for the treatment of acne

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

if you

  • have very sensitive skin
  • are sensitive to benzoyl peroxide

When using this product 

OTC - WHEN USING SECTION

  • skin irritation and dryness is more likely to occur if you use another topical acne medication at the same time.  If irritation occurs, only use one topical acne medication at a time.
  • avoid unnecessary sun exposure and use a sunscreen
  • avoid contact with the eyes, lips and mouth
  • avoid contact with hair and dyed fabrics, which may be bleaced by this product
  • skin irritation may occur, characterized by redness, burning, itching, peeling or possible swelling.  Irritation may be reduced by using the product less frequently or in a lower concentration

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation becomes severe

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.  Avoid contact with eyes.  If contact occurs, flush thoroughly with water.

Directions

DOSAGE & ADMINISTRATION SECTION

  • wet face. Gently massage all over face for 20-30 seconds avoiding the eyes.   Rinse thoroughly and pat dry.
  • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor
  • if bothersome dryness or peeling occurs, reduce daily application to once a day or every other day
  • if going outside, apply sunscreen after using this product.  If irritation or sensitivity develops stop use of both products and ask a doctor
  • Sensitivity Test for a New User.  Apply product sparingly to one or two small affected areas, during the first 3 days.  If no discomfort occurs, follow the directions stated above.

Other information

OTHER SAFETY INFORMATION

  • keep tightly closed
  • store at room temperature (59⁰-77⁰)

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cetyl alcohol, petrolatum, acrylates/C10-30 alkyl acrylate crosspolymer, zinc lactate, steareth-2, glycerin, potassium cetyl phosphate, xanthan gum, benzyl alcohol, fragrance, disodium EDTA, laureth-4, BHT, sodium hydroxide, lactic acid, menthol

Adverse reaction

ADVERSE REACTIONS SECTION

*This product is not manufactured or distributed by Johnson & Johnson Consumer Products Company, distributor of Clean & Clear Continuous Control Acne Cleanser

DISTRIBUTED BY OLD EAST MAIN CO.

100 MISSION RIDGE

GOODLETTSVILLE, TN 37072

100% Satisfaction Guaranteed! (888) 309-9030

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

STUDIO

SELECTION

ACNE

CONTROL

CLEANSER

ACNE

MEDICATION

BENZOYL PEROXIDE 10%

Compare to Clean & Clear

Continuous Control Acne Cleanser

Provides daily control

  • Cleanser for acne prone skin
  • Helps fight blemishes

NET WT 5 OZ (141 g)

image descriptionimage description

Products#

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

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55910-26455910-264-56

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
2ea8a932-3778-ea39-e063-6294a90a281cda4229f0-a3bf-43ce-b5c2-6195a72700262025-02-21Warnings, Adverse reactionsExact identifier
spl set id: da4229f0-a3bf-43ce-b5c2-6195a7270026

Reported adverse events (FAERS/openFDA)#

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