SKINPRINT ACNE RELEASE- skinprint acne release lotion
The Skin Atelier, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Active Ingredient: 2.5% Benzoyl Peroxide

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

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

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.

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

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

SKINPRINT ACNE RELEASE
skinprint acne release lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71393-009
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	2.5 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
TRICAPRYLIN (UNII: 6P92858988)
MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
LAURETH-7 (UNII: Z95S6G8201)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
DIMETHICONE 200 (UNII: RGS4T2AS00)
LAURETH-23 (UNII: N72LMW566G)
LAURETH-4 (UNII: 6HQ855798J)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
GLYCERIN (UNII: PDC6A3C0OX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
WATER (UNII: 059QF0KO0R)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71393-009-50	50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	08/06/2009

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		08/06/2009	10/11/2019

Labeler - The Skin Atelier, Inc. (135049810)

Name	Address	ID/FEI	Business Operations
Establishment
The Skin Atelier, Inc.		135049810	manufacture(71393-009)

Revised: 1/2020

Document Id: 9c58daad-3810-a602-e053-2a95a90a2f93

Set id: 59b8db2c-dbc4-d6d7-e053-2991aa0a07dd

Version: 2

Effective Time: 20200117

The Skin Atelier, Inc.