Label: MELAMIX SKIN LIGHTENER AND BLENDING- hydroquinone cream
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Contains inactivated NDC Code(s)
NDC Code(s): 42851-031-32, 42851-031-80 - Packager: ZO Skin Health, Inc.
- Category: HUMAN PRESCRIPTION DRUG LABEL
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Drug Label Information
Updated April 8, 2014
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- Official Label (Printer Friendly)
- DESCRIPTION
- INDICATIONS & USAGE
- DOSAGE AND ADMINISTRATION
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WARNINGS
Keep out of reach of children.
Contains Sodium Metabisulfite, a sulfite that may cause serious allergic-type reactions including anaphylactic symptoms (e.g. hives, itching), and life threatening or less severe asthmatic episodes in certain susceptible persons.
Some users may experience a mild skin irritation. If skin irritation becomes severe, stop use and consult a physician.
- STORAGE
- ACTIVE INGREDIENT
- INACTIVE INGREDIENTS
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 80 g Bottle Carton
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INGREDIENTS AND APPEARANCE
MELAMIX SKIN LIGHTENER AND BLENDING
hydroquinone creamProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:42851-031 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Hydroquinone (UNII: XV74C1N1AE) (Hydroquinone - UNII:XV74C1N1AE) Hydroquinone 0.04 g in 1 g Inactive Ingredients Ingredient Name Strength Ascorbic Acid (UNII: PQ6CK8PD0R) Butylated Hydroxytoluene (UNII: 1P9D0Z171K) Cetyl Alcohol (UNII: 936JST6JCN) Edetate Disodium (UNII: 7FLD91C86K) Ethylhexyl Palmitate (UNII: 2865993309) Glycerin (UNII: PDC6A3C0OX) Glycolic Acid (UNII: 0WT12SX38S) Methylparaben (UNII: A2I8C7HI9T) Phenyl Trimethicone (UNII: DR0K5NOJ4R) Propylparaben (UNII: Z8IX2SC1OH) Water (UNII: 059QF0KO0R) CAULOSIDE D (UNII: 4N5Z068GAZ) Sodium Lauryl Sulfate (UNII: 368GB5141J) Sodium Metabisulfite (UNII: 4VON5FNS3C) .Alpha.-Tocopherol Acetate (UNII: 9E8X80D2L0) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:42851-031-80 1 in 1 CARTON 1 80 g in 1 BOTTLE, PLASTIC 2 NDC:42851-031-32 1 in 1 CARTON 2 32 g in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date UNAPPROVED DRUG OTHER 01/01/2012 Labeler - ZO Skin Health, Inc. (826468527) Establishment Name Address ID/FEI Business Operations Sanitor Coporation 797472792 MANUFACTURE(42851-031)