FDA.reportPublic FDA data

Skinprint Acne Release

Manufacturer
The Skin Atelier, Inc.
Effective date
2009-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:11:53

Label at a glance#

ProductSkinprint Acne Release
Active ingredientBENZOYL PEROXIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: 2.5% Benzoyl Peroxide

INSTRUCTIONS FOR USE SECTION

Use twice daily after thoroughly cleansing skin. Apply all over face until lotion disappears.

DOSAGE & ADMINISTRATION SECTION

Directions: Use twice daily after thoroughly cleansing skin. Apply all over face until lotion disappears.

WARNINGS SECTION

Warning: For external use only. When using this product avoid contact with eyes. If contact occures, flush thoroughly with water. Keep out of the reach of children. If swallowed get medical help or contact Poison Control Center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warning: For external use only. When using this product avoid contact with eyes. If contact occures, flush thoroughly with water. Keep out of the reach of children. If swallowed get medical help or contact Poison Control Center right away.

INACTIVE INGREDIENT SECTION

WATER, CYCLOPENTASILOXANE, DIMETHICONE CROSSPOLYMER, DIMETHICONE, LAURETH-23, LAURETH-4, SODIUM HYALURONATE, GLYCERIN, POLYETHYLENE, SODIUM POLYACRYLATE, POLYACRYLAMIDE, C-13-14 ISOPARRAFIN, LAURTEH 7, PHENOXYETHANOL, CAPRYLL GLYCOL, POTASSIUM SORBATE, HEXYLENE GLYCOL, BISABOLOL, ZINGIBER OFFICINALE (GINGER ROOT) EXTRACT, CAPRIC CAPRYLIC TRIGYLCERIDE, DISODIUM EDTA

INDICATIONS & USAGE SECTION

This lotion clears the skin with a new BPO formula that more effectively gets into pores while minimizing irritation.

OTC - PURPOSE SECTION

This lotion clears the skin with a new BPO formula that more effectively gets into pores while minimizing irritation.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label_AcneReleaseLotion.jpgLabel_AcneReleaseLotion.jpg

Products#

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

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71393-00971393-009-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYACRYLAMIDE (10000 MW)E2KR9C9V2IIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
TRICAPRYLIN6P92858988IACT
MAGNESIUM DISODIUM EDTANDT563S5VZIACT
SODIUM POLYACRYLATE (2500000 MW)05I15JNI2JIACT
C13-14 ISOPARAFFINE4F12ROE70IACT
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMERRSA9I561OKIACT
DIMETHICONE 200RGS4T2AS00IACT
LAURETH-23N72LMW566GIACT
LAURETH-46HQ855798JIACT
HYALURONATE SODIUMYSE9PPT4THIACT
GLYCERINPDC6A3C0OXIACT
LAURETH-7Z95S6G8201IACT
PHENOXYETHANOLHIE492ZZ3TIACT
HEXYLENE GLYCOLKEH0A3F75JIACT
.ALPHA.-BISABOLOL, (+/-)-36HQN158VCIACT
ZINGIBER OFFICINALE WHOLEIN6Q3S3414IACT
CAPRYLYL GLYCOL00YIU5438UIACT
BENZOYL PEROXIDEW9WZN9A0GMACTIB
WATER059QF0KO0RIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT

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
59b8db2c-dbc5-d6d7-e053-2991aa0a07dd59b8db2c-dbc4-d6d7-e053-2991aa0a07dd2009-08-06WarningsExact identifier
spl id: 59b8db2c-dbc5-d6d7-e053-2991aa0a07dd
spl set id: 59b8db2c-dbc4-d6d7-e053-2991aa0a07dd

Reported adverse events (FAERS/openFDA)#

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