SKINPRINT SPOT-ON- skinprint spot-on 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: Benzoyl Peroxide 5%

Apply to affected area as needed.

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

WATER, CYCLOPENTASILOXANE, DIMETHICONE CROSSPOLYMER, DIMETHICONE, LAURETH-23, LAURETH-4, GLYCERIN, BUTYLENE GLYCOL, CAMELLIA SINENSIS (TEA) EXTRACT, ASALATHUS LINEARIS (ROOIBOS) EXTRACT, BOSWELLIA SERRATA EXTRACT, HONEY EXTRACT, TETRAPEPTIDE-14, PHENOXYETHANOL, SODIUM BENZOATE, SODIUM POLYACRYLATE, SODIUM HYALURONATE, CAPRYL CAPRYLIC TRIGLYCERIDES, POLYETHYLENE, BISABOLOL, ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, CAPRYLYL GLYCOL, CAPRYLHYDROXAMIC ACID, POLYACRYLAMIDE, C13-14 ISOPARRAFIN, LAURETH-7, DISODIUM EDTA, SODIUM STEAROYL LACTYLATE, CETYL ALCOHOL, OLUS/VEGETABLE OIL, TOCOPHERYL ACETATE, GLYCINE SOJA/GLYCINE (SOYBEAN) STEROLS, SODIUM CARBOXYMETHYL BETAGLUCAN, SODIUM LACTATE, CARNOSINE, LACTIC ACID

Reduces blemishes & pimples with new small particle Benzoyl Peroxide to get into pores more effectively.

SKINPRINT SPOT-ON
skinprint spot-on lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71393-010
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
BENZOYL PEROXIDE (UNII: W9WZN9A0GM) (BENZOYL PEROXIDE - UNII:W9WZN9A0GM)	BENZOYL PEROXIDE	5 g in 100 g

Ingredient Name	Strength
Inactive Ingredients
WATER (UNII: 059QF0KO0R)
DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK)
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
CETYL ALCOHOL (UNII: 936JST6JCN)
SOY STEROL (UNII: PL360EPO9J)
SODIUM CARBOXYMETHYL .BETA.-GLUCAN (DS 0.65-0.85) (UNII: 2YGO1190AP)
SODIUM LACTATE (UNII: TU7HW0W0QT)
CARNOSINE (UNII: 8HO6PVN24W)
LACTIC ACID (UNII: 33X04XA5AT)
LAURETH-4 (UNII: 6HQ855798J)
GLYCERIN (UNII: PDC6A3C0OX)
BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ)
TETRAPEPTIDE-15 (UNII: 3PH5M0466G)
SODIUM BENZOATE (UNII: OJ245FE5EU)
DIMETHICONE 200 (UNII: RGS4T2AS00)
LAURETH-23 (UNII: N72LMW566G)
CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)
ASPALATHUS LINEARIS WHOLE (UNII: O17JQA1A9Z)
ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
LAURETH-7 (UNII: Z95S6G8201)
MAGNESIUM DISODIUM EDTA (UNII: NDT563S5VZ)
SODIUM STEAROYL LACTYLATE (UNII: IN99IT31LN)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71393-010-15	15 g in 1 JAR; Type 0: Not a Combination Product	10/08/2012

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		10/08/2012	10/11/2019

Labeler - The Skin Atelier, Inc. (135049810)

Name	Address	ID/FEI	Business Operations
Establishment
The Skin Atelier, Inc.		135049810	manufacture(71393-010)

Revised: 1/2020

Document Id: 9c58b876-9c90-5807-e053-2995a90a20cb

Set id: 5cedc020-4f99-5f08-e053-2991aa0a1659

Version: 2

Effective Time: 20200117

The Skin Atelier, Inc.