FDA.reportPublic FDA data

Clean And Clear Continuous Control Acne Cleanser

Manufacturer
Johnson & Johnson Consumer Inc.
Effective date
2023-01-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 21:39:02

Label at a glance#

ProductClean And Clear Continuous Control Acne Cleanser
Active ingredientBENZOYL PEROXIDE
Label structure11 sections

Dosage and administration

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

Storage and handling

Keep tightly closed Store at 20°C to 25°C (68°F - 77°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl Peroxide 10%

Purpose

OTC - PURPOSE SECTION

Acne treatment

Use

INDICATIONS & USAGE SECTION

  • For the treatment of acne.

Warnings

WARNINGS SECTION

For external use only.

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. If contact occurs, flush thoroughly with water
  • avoid contact with hair or dyed products, which may be bleached 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.

OTC - DO NOT USE SECTION

Do not use if you

  • have very sensitive skin
  • are sensitive to benzoyl peroxide.

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • Irritation becomes severe.

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 face. Gently massage all over face for 20 – 30 seconds, avoiding eye area. Rinse thoroughly and pat dry.
  • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two times daily if needed or as directed by a doctor.
  • If bothersome dryness or peeling occurs, reduce 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.

Other Information

STORAGE AND HANDLING SECTION

  • Keep tightly closed
  • Store at 20°C to 25°C (68°F - 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cetyl Alcohol, Petrolatum, Glycerin, Steareth-2, Zinc Lactate, Potassium Cetyl Phosphate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Xanthan Gum, Benzyl Alcohol, Fragrance, Laureth-4, Disodium EDTA, BHT, Menthol

Questions?

OTC - QUESTIONS SECTION

Call toll-free 877-754-6411 or 215-273-8755 (collect) or visit www.CleanandClear.com

SPL UNCLASSIFIED SECTION

Distributed in the US by:
JOHNSON & JOHNSON CONSUMER INC.
Skillman, NJ 08558

PRINCIPAL DISPLAY PANEL - 142 g Tube Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Clean
&
Clear ®
continuous
control ®
acne cleanser
10% benzoyl peroxide acne treatment
DAILY FORMULA
after one week of use,
skin is visibly clearer
and less oily

NET WT. 5 OZ. (142 g)

PRINCIPAL DISPLAY PANEL - 142 g Tube Label
PRINCIPAL DISPLAY PANEL - 142 g Tube Label

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69968-068469968-0684-5

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
CETYL ALCOHOL936JST6JCNIACT
PETROLATUM4T6H12BN9UIACT
GLYCERINPDC6A3C0OXIACT
STEARETH-2V56DFE46J5IACT
ZINC LACTATE2GXR25858YIACT
POTASSIUM CETYL PHOSPHATE03KCY6P7UTIACT
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)59TL3WG5COIACT
XANTHAN GUMTTV12P4NEEIACT
BENZYL ALCOHOLLKG8494WBHIACT
LAURETH-46HQ855798JIACT
EDETATE DISODIUM7FLD91C86KIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
BENZOYL PEROXIDEW9WZN9A0GMACTIB

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
f3080b43-b10c-41a4-e053-2995a90a94194a4e78c3-984b-4374-94dd-9aa9a1ba78802023-01-24WarningsExact identifier
spl id: f3080b43-b10c-41a4-e053-2995a90a9419
spl set id: 4a4e78c3-984b-4374-94dd-9aa9a1ba7880

Reported adverse events (FAERS/openFDA)#

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