RECOVER LIGHTENING COMPLEX WITH 4% HYDROQUINONE- recover lightening complex with 4% hydroquinone 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: 4% HYDROQUINONE

gently smooth over entire face. Let product absorb at least 2 minutes before applying lotion.

Gently smooth over entire face. Let product absorb at least 2 minutes before applying lotion.

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

WATER, ETHANOL SD 39C, POLYETHYLENE, SODIUM POLYACRYLATE , PPG-3 BENZYL ETHER 2 ETHYLHEXANOATE, POLYACRYLAMIDE, C13- 14 ISOPARAFIN, LAURETH-7, GLYCERIN, BUTYLENE GLYCOL, PENTYLENE GLYCOL, HYDROXYPHENYL PROPAMIDOBENZOIC ACID, TRIETHANOLAMINE, UNDECYLENOYL PHENYLALANINE, SODIUM PALMITOYL PROLINE, NUMPHAEA ALBA FLOWER EXTRACT, GLYCOLIC ACID, BISABOLOL, ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, PHENOXYETHANOL, CAPRYLYL GLYCOL, POTASSIUM SORBATE, HEXYLENE GLYCOL, DIMETHYLMETHOXY CHROMANYL PALMITATE, DISODIUM EDTA, SODIUM METABISULFITE, FRAGRANCE

This lightening treatment lightens the skin with minimal irritation. Brightens sun damage, Melasma and dark spots on skin.

This lightening treatment lightens skin with minimal irritation. Brightens sun damage, Melasma and dark spots on skin.

Keep out of reach of children. If swallowed get medial help or contact Poison Control Center right away.

RECOVER LIGHTENING COMPLEX WITH 4% HYDROQUINONE
recover lightening complex with 4% hydroquinone lotion

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:71393-004
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	0.04 g in 1 g

Ingredient Name	Strength
Inactive Ingredients
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
SODIUM PALMITOYL PROLINE (UNII: 64L053FRFO)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
TROLAMINE (UNII: 9O3K93S3TK)
NYMPHAEA ALBA FLOWER (UNII: 40KQ7Q535O)
GLYCOLIC ACID (UNII: 0WT12SX38S)
.ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)
ZINGIBER OFFICINALE WHOLE (UNII: IN6Q3S3414)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
UNDECYLENOYL PHENYLALANINE (UNII: 271P08C6OD)
ALCOHOL (UNII: 3K9958V90M)
C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
LAURETH-7 (UNII: Z95S6G8201)
GLYCERIN (UNII: PDC6A3C0OX)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
HYDROXYPHENYL PROPAMIDOBENZOIC ACID (UNII: 25KRT26H77)
POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
PPG-3 BENZYL ETHER MYRISTATE (UNII: 8075L58MKO)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
WATER (UNII: 059QF0KO0R)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
DIMETHYLMETHOXY CHROMANYL PALMITATE (UNII: 5G222ZDK7U)
DISODIUM HEDTA (UNII: KME849MC7A)
LOW DENSITY POLYETHYLENE (UNII: J245LN42AI)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:71393-004-50	50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	02/16/2011

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved drug other		02/16/2011	10/11/2019

Labeler - The Skin Atelier, Inc. (135049810)

Name	Address	ID/FEI	Business Operations
Establishment
The Skin Atelier, Inc.		135049810	manufacture(71393-004)

Revised: 1/2020

Document Id: 9c58e7f8-abbb-56a2-e053-2995a90a1f82

Set id: 5048b657-38e6-22f7-e054-00144ff8d46c

Version: 2

Effective Time: 20200117

The Skin Atelier, Inc.