Skin Perfecting Acne and Blemish Wash

Manufacturer
Biocosmetics Research Labs
Effective date
2006-06-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:19

Label at a glance#

ProductSkin Perfecting Acne and Blemish Wash
Active ingredientSalicylic Acid
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Salicylic Acid 0.50%

OTC - PURPOSE SECTION


Purpose:

Acne Treatment Wash

INDICATIONS & USAGE SECTION


Use:

For the treatment of acne.  Clears up most of the acne blemishes, acne pimples, blackheads and 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 twice daily, rinse with warm water.

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, Sodium Laureth Sulfate, Disodium Laureth Sulfosuccinate, Acrylates/C10-30 Alkyl Acrylates Copolymer, Propylene Gylcol, Polysorbate 20, Microcellulose, Lactose, Tocopheryl Acetate, Retinyl Palmitate, Urtica Dioica (Nettle) Extract, Salix Alba (Willow) Bark Extract, Hamamelis Virginiana (Witch Hazel) Extract, Microcrystalline Cellulose, Triclosan, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Benzophenone-4, Sodium hydroxide, Fragrance, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Ultramarines (CI 77007).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of acnewash cartonImage of acnewash carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
199308salicylic acid 0.5 % Topical SolutionPSN1
199308salicylic acid 5 MG/ML Topical SolutionSCD1
199308salicylic acid 0.5 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59735-314-062020-01-31C16284748780-19d75b9d0-303a-f424-e053-dadaa90a57ceSkin Perfecting Acne and Blemish Wash

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59735-314-06Skin Perfecting Acne and Blemish Wash180 mL in 1 BOTTLE, PLASTICRINSE1801
59735-314-06Skin Perfecting Acne and Blemish Wash1 in 1 CARTONRINSE11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59735-314SKIN PERFECTING ACNE AND BLEMISH WASH (SALICYLIC ACID) RINSE [BIOCOSMETICS RESEARCH LABS]1Legacy NDC, 2 package rows20100724_772bf90a-e764-40c0-8b31-299cfbc4146e.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
59735-31459735-314-06

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
7ebadcb8-7c7b-4409-8653-900b361ecc54772bf90a-e764-40c0-8b31-299cfbc4146e2006-06-19WarningsExact identifier
spl id: 7ebadcb8-7c7b-4409-8653-900b361ecc54
spl set id: 772bf90a-e764-40c0-8b31-299cfbc4146e

Reported adverse events (FAERS/openFDA)#

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