HQ PLUS BRIGHTENING CREAM VI DERM- hydroquinone cream

HQ Plus Brightening Cream by

Drug Labeling and Warnings

HQ Plus Brightening Cream by is a Otc medication manufactured, distributed, or labeled by Vi Medical Products Inc., VEGE-KURL, INC, VEGE-KURL, INC . Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient                    Purpose

Hydroquinone 2.0%                 Skin Brightening

PURPOSE

Use

• Skin brightening formula that may help reduce discolorations

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed seek medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Stop and ask a doctor if skin irritation becomes severe

WARNINGS

Warning

• For External Use only. When using this product: avoid unnecessary sun exposure and use a suncreen
• Some Users of this product may experience a mild irritation
• Do not use on children under 12 years of age, unless directed by a doctor

DOSAGE & ADMINISTRATION

Directions

• Cleanse the skin thoroughly before use. Cover the affected area with thin layer morning and night. Use Sunscreen daily. We recommend VI Derm SPF50+

INACTIVE INGREDIENT

Water (Aqua), Propylene Glycol, Caprylic/Capric Triglyceride, Glyceryl Stearate, Isopropyl Palmitate, Butylene Glycol, Glycerin, PEG-100 Stearate, Cetearyl Alcohol, Azelaic Acid, Cetyl Phosphate, Triethanolamine, Arbutin, Fragrance, Kojic Acid, Rumex Occidentalis Extract, Ascorbic Acid, Dicetyl Phosphate, Ceteth-10 Phosphate, Sodium Ascorbyl Phosphate, Dimethicone, Bisabolol, Glycyrrhiza Glabra (Licorice) Root Extract, Sodium Metabisulfite, Zea Mays (Corn) Oil, BHT, Lactic Acid, Xanthan Gum, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Tetrasodium EDTA, Ethylhexylglycerin, Phenoxyethanol

PRINCIPAL DISPLAY PANEL

VI Derm HQ Plus

Brightening Cream

1.75 FL OZ/50 mL

INGREDIENTS AND APPEARANCE

HQ PLUS BRIGHTENING CREAM  VI DERM
hydroquinone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70484-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	1 g  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
GLYCERIN (UNII: PDC6A3C0OX)
PEG-100 STEARATE (UNII: YD01N1999R)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
AZELAIC ACID (UNII: F2VW3D43YT)
CETYL PHOSPHATE (UNII: VT07D6X67O)
TROLAMINE (UNII: 9O3K93S3TK)
ARBUTIN (UNII: C5INA23HXF)
KOJIC ACID (UNII: 6K23F1TT52)
ASCORBIC ACID (UNII: PQ6CK8PD0R)
DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
DIMETHICONE (UNII: 92RU3N3Y1O)
LEVOMENOL (UNII: 24WE03BX2T)
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
CORN OIL (UNII: 8470G57WFM)
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
LACTIC ACID (UNII: 33X04XA5AT)
XANTHAN GUM (UNII: TTV12P4NEE)
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
EDETATE SODIUM (UNII: MP1J8420LU)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
PHENOXYETHANOL (UNII: HIE492ZZ3T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70484-004-02	1 in 1 BOX	07/05/2016
1	NDC: 70484-004-01	50 mL in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part358A	07/05/2016

Labeler - Vi Medical Products Inc. (063910521)

Establishment
Name	Address	ID/FEI	Business Operations
VEGE-KURL, INC		021072509	manufacture(70484-004)