FDA.reportPublic FDA data

Acne Control

Manufacturer
Walgreen | APOLLO HEALTH AND BEAUTY CARE
Effective date
2023-09-11
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:56:28

Label at a glance#

ProductAcne Control
Active ingredientSALICYLIC ACID
Label structure7 sections

Indications and uses

For the treatment of acne.

Dosage and administration

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. Rinse off after use. Sensitivity Test for a New user. Apply product sparingl...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2%

Purpose

OTC - PURPOSE SECTION

Acne Treatment

Uses

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 drynessis 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.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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.
  • Rinse off after use.

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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropyl hydroxysultaine, Glycerin, Sodiumj Lauroyl sarcosinate, Sodium Methyl Cocvoyl Taurate, PEG-150 Pentaerythrityl Tetrastearate, Niacinamide, Ceramide NP, Ceramide AP, Ceramide EOP, Carbomer, Phytosphingosine, Cholesterol, Sodium Lauroyl Lactylate, Hydrolyzed Hyaluronic Acid, Disodium EDTA, Benzyl alcohol, Ethylhexylglycerin, Tocopherol, Xanthan gum, Citric Acid, Sodium Hydroxide.

Label Copy

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
562600salicylic acid 2 % Medicated Liquid SoapPSN5
562600salicylic acid 20 MG/ML Medicated Liquid SoapSCD5
562600salicylic acid 2 % Facial Cleanser TonerSY5
562600salicylic acid 2 % Facial ScrubSY5
562600salicylic acid 2 % Medicated Liquid SoapSY5

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130195602087464GTIN-13: 0195602087464
EAN-13: 0195602087464
GTIN-12: 195602087464
UPC-A: 195602087464
GTIN storage (14 digits): 00195602087464		0363-5834-08.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-5834-08Acne Control236 mL in 1 BOTTLE, PLASTICCREAM2365

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
0363-58340363-5834-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
CARBOMER0A5MM307FCIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHYTOSPHINGOSINEGIN46U9Q2QIACT
TOCOPHEROLR0ZB2556P8IACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
SODIUM LAUROYL SARCOSINATE632GS99618IACT
PEG-150 PENTAERYTHRITYL TETRASTEARATE8L4OOQ76AMIACT
CERAMIDE APF1X8L2B00JIACT
CHOLESTEROL97C5T2UQ7JIACT
SODIUM METHYL COCOYL TAURATEJVL98CG53GIACT
NIACINAMIDE25X51I8RD4IACT
SODIUM LAUROYL LACTYLATE7243K85WFOIACT
CERAMIDE 15THT33P7X7IACT
HYALURONIC ACIDS270N0TRQYIACT
EDETATE DISODIUM7FLD91C86KIACT
BENZYL ALCOHOLLKG8494WBHIACT
SODIUM HYDROXIDE55X04QC32IIACT
XANTHAN GUMTTV12P4NEEIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
CERAMIDE NP4370DF050BIACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
Acne ControlCREAMWalgreenfc60cccb-405b-e49e-e053-6394a90a5a122023-09-11WarningsExact identifier
ndc (package): 0363-5834-08
ndc (product): 0363-5834
ndc11 (package): 00363583408
spl id: 50ebf315-d555-359d-e063-6394a90a0529
spl set id: fc60cccb-405b-e49e-e053-6394a90a5a12

Reported adverse events (FAERS/openFDA)#

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