Anti-acne Lotion

Manufacturer
Biocosmetics Research Labs
Effective date
2008-01-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:18

Label at a glance#

ProductAnti-acne
Active ingredientSalicylic Acid
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


Active Ingredient:

Salicylic Acid 2%

OTC - PURPOSE SECTION


Purpose:

Acne Treatment Cream

INDICATIONS & USAGE SECTION

Use:For the treatment of acne.  Clears up most of the acne blemishes, acne pimples, blackheads or whiteheads.

WARNINGS SECTION


Warnings: 

For external use only.

Using other topical acne medications at the same time or immediately following use of this product may increase dryness or irritation of the skin.  If this occurs, only one medication should be used unless directed by a doctor.

DOSAGE & ADMINISTRATION SECTION


Directions:

Cleanse the skin thoroughly before applying the medication.  Cover the entire affected area with a thin layer 1-2 times daily.  Because excessive drying of the skin may occur, start with one application every other day, then gradually increase.  If bothersome dryness or peeling occurs, reduce application to once every other few days.

PRECAUTIONS SECTION


Sensitivity test for 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.

INACTIVE INGREDIENT SECTION


Other Ingredients:

Water, Methyl Gluceth-20, Isopropyl Myristate, Sorbitan Stearate, Cetyl Alcohol, Alcohol Denat, Triethanolamine, Caprylic/Capric Triglyceride, Dimethicone,
Sodium Polyacrylate, Ceteareth-20, Butylene Glycol, Ethylhexyl Stearate, Capryloyl Glycine, Sarcosine, Cinnamomum Zeylanicum Bark Extract, Mel (Honey Extract), Trideceth-6, Retinyl Palmitate, Tocopheryl Acetate, Hydroxyethylcellulose, Arnica Montana Flower Extract, Xanthan Gum, Disodium EDTA, Diazolidinyl Urea, Iodopropynyl Butylcarbamate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton for Anti Acne LotionImage of carton for Anti Acne Lotion

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
103568salicylic acid 2 % Topical LotionPSN1
103568salicylic acid 20 MG/ML Topical LotionSCD1
103568salicylic acid 2 % Topical LotionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59735-312-562020-01-31C16284748780-19d75b9cf-f164-f424-e053-dadaa90a57ceAnti-acne Lotion

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59735-312-56Anti-acne1 in 1 CARTONLOTION11
59735-312-56Anti-acne56.8 g in 1 TUBELOTION56.81

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59735-312ANTI-ACNE (SALICYLIC ACID) LOTION [BIOCOSMETICS RESEARCH LABS]1Legacy NDC, 2 package rows20100723_05d699ae-a3d3-4da0-b5fc-cd872ec04713.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Salicylic AcidACTIVE INGREDIENTO414PZ4LPZ1
Salicylic AcidACTIVE MOIETYO414PZ4LPZ1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59735-31259735-312-56

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
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
1d33bb86-a544-4fdc-9f16-c76b848ab30305d699ae-a3d3-4da0-b5fc-cd872ec047132008-01-23WarningsExact identifier
spl id: 1d33bb86-a544-4fdc-9f16-c76b848ab303
spl set id: 05d699ae-a3d3-4da0-b5fc-cd872ec04713

Reported adverse events (FAERS/openFDA)#

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