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Recover Lightening Complex Prescribing Information

Package insert / product label
Generic name: hydroquinone
Dosage form: lotion
Drug class: Topical depigmenting agents

Medically reviewed by Drugs.com. Last updated on Mar 25, 2024.

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.

Recover4HQ.jpg

RECOVER LIGHTENING COMPLEX WITH 4% HYDROQUINONE
recover lightening complex with 4% hydroquinone lotion
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:71393-004
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE0.04 g in 1 g
Inactive Ingredients
Ingredient NameStrength
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)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
WATER (UNII: 059QF0KO0R)
SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)
PPG-3 BENZYL ETHER MYRISTATE (UNII: 8075L58MKO)
DIMETHYLMETHOXY CHROMANYL PALMITATE (UNII: 5G222ZDK7U)
DISODIUM HEDTA (UNII: KME849MC7A)
LOW DENSITY POLYETHYLENE (UNII: J245LN42AI)
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71393-004-5050 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product02/16/2011
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/16/2011
Labeler - The Skin Atelier, Inc. (135049810)
Establishment
NameAddressID/FEIBusiness Operations
The Skin Atelier, Inc.135049810manufacture(71393-004)

Medical Disclaimer