Label: HQ PLUS BRIGHTENING CREAM VI DERM- hydroquinone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 70484-004-01, 70484-004-02 - Packager: Vi Medical Products Inc.
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated February 14, 2020
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- WARNINGS
- DOSAGE & ADMINISTRATION
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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
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INGREDIENTS AND APPEARANCE
HQ PLUS BRIGHTENING CREAM VI DERM
hydroquinone creamProduct 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)