Acne Control Cleanser

Manufacturer
Rite Aid | Consumer Product Partners, LLC
Effective date
2025-06-30
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
legacy-cache
Hydrated at
2026-08-01 20:36:23

Label at a glance#

ProductAcne Control Cleanser
Active ingredientBENZOYL PEROXIDE
Label structure14 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 u...

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 if you

OTC - DO NOT USE SECTION

  • 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 possibly 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 (59⁰-77⁰F)

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

Disclaimer

SPL UNCLASSIFIED SECTION

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

ADVERSE REACTION

ADVERSE REACTIONS SECTION

Distributed By: RITE AID

30 HUNTER LANE, CAMP HILL, PA 17011

www.riteaid.com

TIME TO SHINE GUARANTEE

If you are not satisifed, we will happily refund your money.

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DAILY

ACNE

CONTROL

CLEANSER

DAILY CONTROL

10% BENZOYL PEROXIDE ACNE MEDICATION

KEEPS FIGHTING ACNE AFTER YOU WASH

RYSHI™

COMPARE TO Clean & Clear ®Continuous Control ®Acne Cleanser*

NET WT 5 OZ (141 g)

image descriptionimage description

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11822-618411822-6184-0

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
40083c9d-f68a-b172-e063-6294a90a20302de6913d-49e5-4e75-9508-d7668749431b2025-09-30Warnings, Adverse reactionsExact identifier
spl set id: 2de6913d-49e5-4e75-9508-d7668749431b

Reported adverse events (FAERS/openFDA)#

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