Walgreens Acne Foaming Cream Cleanser

Manufacturer
WALGREEN COMPANY
Effective date
2026-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-03 03:03:56

Label at a glance#

ProductWalgreens Acne Foaming Cleanser
Active ingredientBENZOYL PEROXIDE
Label structure11 sections

Indications and uses

for the treatment of acne

Dosage and administration

Cover the entire affected area with a thin layer, massage gently one to two minutes, and rinse thoroughly with water one to three times a day Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three 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 ou...

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzoyl peroxide 4.0%

Purpose

OTC - PURPOSE SECTION

Acne Medication

Uses

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

  • avoid contact with the eyes, lips, and mouth
  • avoid unnecessary sun exposure and use a sunscreen
  • avoid contact with hair and dyed fabrics 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.
  • 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.

Stop use and ask doctor if

OTC - STOP USE SECTION

  • irritation becomes severe.

Keep out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Cover the entire affected area with a thin layer, massage gently one to two minutes, and rinse thoroughly with water one to three times a day
  • Because excessive drying of the skin may occur, start with one application daily, then gradually increase to two to three 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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

benzoic acid, carbomer, ceramide AP, ceramide EOP, ceramide NP, cholesterol, cocamidopropyl hydroxysultaine, ethylhexylglycerin, glycerin, glycolic acid, niacinamide, phytosphingosine, potassium hydroxide, propanediol, propylene glycol, sodium chloride, sodium citrate, sodium C14-16 olefin sulfonate, sodium hyaluronate, sodium lauroyl lactylate, tocopheryl acetate, water, xanthan gum.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

W85255AW85255A

W85255A

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-13640363-1364-23

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 24 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
Walgreens Acne Foaming CleanserBENZOYL PEROXIDEWALGREEN COMPANY549fddb8-9d42-16cb-e063-6294a90aa2a92026-06-19WarningsExact identifier
ndc (package): 0363-1364-23
ndc (product): 0363-1364
ndc11 (package): 00363136423
spl id: 549fea8d-70bb-ad68-e063-6294a90a48a8
spl set id: 549fddb8-9d42-16cb-e063-6294a90aa2a9

Reported adverse events (FAERS/openFDA)#

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