SKIN LIGHTENING COMPLEX- hydroquinone cream

SKIN LIGHTENING COMPLEX by

Drug Labeling and Warnings

SKIN LIGHTENING COMPLEX by is a Prescription medication manufactured, distributed, or labeled by Vi Medical Products Inc., Vi Medical Products Inc. INC, MICRO CONNECTION ENTERPRISES INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

USE

HELPS LIGHTEN DARK PATCHES OF SKIN SUCH AS AGE SPOTS, MELASMA, FRECKLES AND HYPERPIGMENTATION THAT CAN OCCUR AS A RESULT OF PREGNANCY, USE OF ORAL CONTRACEPTIVES OR INJURY TO THE SKIN. RX ONLY. FOR EXTERNAL USE ONLY.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SKIN LIGHTENING COMPLEX 
hydroquinone cream

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 70484-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	4 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ARBUTIN (UNII: C5INA23HXF)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
AZELAIC ACID (UNII: F2VW3D43YT)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
GREEN TEA LEAF (UNII: W2ZU1RY8B0)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
CETYL ALCOHOL (UNII: 936JST6JCN)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
DIMETHICONE (UNII: 92RU3N3Y1O)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
KOJIC DIPALMITATE (UNII: 13N249RWTM)
MALIC ACID (UNII: 817L1N4CKP)
MALVA SYLVESTRIS FLOWERING TOP (UNII: X1U1U0N90J)
METHYL HYDROGENATED ROSINATE (UNII: 13DHA19W9N)
PEG-100 STEARATE (UNII: YD01N1999R)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
EDETATE SODIUM (UNII: MP1J8420LU)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70484-101-12	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	07/29/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		07/28/2019

Labeler - Vi Medical Products Inc. (063910521)

Registrant - Vi Medical Products Inc. INC (063910521)

Establishment
Name	Address	ID/FEI	Business Operations
MICRO CONNECTION ENTERPRISES INC		144297160	manufacture(70484-101)