FDA.reportPublic FDA data

Walgreens Acne Control Gel

Manufacturer
WALGREEN COMPANY
Effective date
2024-10-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:25:29

Label at a glance#

ProductWalgreens Acne Control Gel
Active ingredientSALICYLIC ACID
Label structure10 sections

Indications and uses

For the treatment of acne clears acne blemishes and allows skin to heal helps prevent new acne blemishes from forming

Dosage and administration

cleanse the skin thoroughly before applying this product. cover the entire affected area with a thin layer one to three times daily. 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 application to once a day or every other day.

Storage and handling

may stain some fabrics

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid 2.0%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

INDICATIONS & USAGE SECTION

  • For the treatment of acne
  • clears acne blemishes and allows skin to heal
  • helps prevent new acne blemishes from forming

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 contact with eyes. If contact occurs, flush thoroughly with water.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • cleanse the skin thoroughly before applying this product.
  • cover the entire affected area with a thin layer one to three times daily.
  • 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 application to once a day or every other day.

Other information

STORAGE AND HANDLING SECTION

  • may stain some fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

behentrimonium methosulfate, carbomer, ceramide AP, ceramide EOP, ceramide NP, cetearyl alcohol, cetyl alcohol, chlorphenesin, cholesterol, disodium EDTA, glycerin, glycolic acid, guar hydroxypropyltrimonium chloride, lactic acid, niacinamide, phytosphingosine, sodium hyaluronate, sodium hydroxide, sodium lauroyl lactylate, water, xanthan gum

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

W08749AW08749A

W08749KW08749K

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
346298salicylic acid 2 % Topical GelPSN2
346298salicylic acid 0.02 MG/MG Topical GelSCD2
346298salicylic acid 2 % Topical GelSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-0269-83Walgreens Acne Control Gel40 mL in 1 TUBEGEL402
0363-0269-83Walgreens Acne Control Gel1 in 1 CARTONGEL12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-0269WALGREENS ACNE CONTROL GEL (SALICYLIC ACID) GEL [WALGREEN COMPANY]2Current NDC, 2 package rows20241016_ffc4c35b-1390-951b-e053-6294a90a1b11.zip

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0363-02690363-0269-83

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
XANTHAN GUMTTV12P4NEEIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
SALICYLIC ACIDO414PZ4LPZACTIB
CHLORPHENESINI670DAL4SZIACT
CHOLESTEROL97C5T2UQ7JIACT
GLYCOLIC ACID0WT12SX38SIACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT
LACTIC ACID33X04XA5ATIACT
PHYTOSPHINGOSINEGIN46U9Q2QIACT
HYALURONATE SODIUMYSE9PPT4THIACT
SODIUM HYDROXIDE55X04QC32IIACT
CETYL ALCOHOL936JST6JCNIACT
SODIUM LAUROYL LACTYLATE7243K85WFOIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
NIACINAMIDE25X51I8RD4IACT
BEHENTRIMONIUM METHOSULFATE5SHP745C61IACT
CERAMIDE APF1X8L2B00JIACT
POLYACRYLIC ACID (8000 MW)73861X4K5FIACT
CERAMIDE NP4370DF050BIACT
EDETATE DISODIUM7FLD91C86KIACT

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 Control GelSALICYLIC ACIDWALGREEN COMPANYffc4c35b-1390-951b-e053-6294a90a1b112024-10-14WarningsExact identifier
ndc (package): 0363-0269-83
ndc (product): 0363-0269
ndc11 (package): 00363026983
spl id: 24729761-e0eb-0a70-e063-6394a90affcf
spl set id: ffc4c35b-1390-951b-e053-6294a90a1b11

Reported adverse events (FAERS/openFDA)#

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