ZO MEDICAL MELAMIN-C SKIN BLEACHING AND CORRECTING WITH VITAMIN C HYDROQUINONE (HYDROQUINONE) CREAM [ZO SKIN HEALTH, INC.]

ZO MEDICAL MELAMIN-C SKIN BLEACHING AND CORRECTING WITH VITAMIN C HYDROQUINONE (HYDROQUINONE) CREAM [ZO SKIN HEALTH, INC.]
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NDC 42851-034-34, 42851-034-85
Set ID 9a1069df-db5d-4ffd-a2da-9137fb7dd4f3
Category HUMAN PRESCRIPTION DRUG LABEL
Packager ZO Skin Health, Inc.
Generic Name
Product Class
Product Number
Application Number
  • SPL UNCLASSIFIED SECTION

    RX ONLY
    FOR EXTERNAL USE ONLY:
    NOT FOR OPHTHALMIC USE

  • DESCRIPTION

    Hydroquinone is 1, 4-benzendiol, with a chemical formula of C6H6O2 and a molecular weight of 110.11.

    The structural formula is:

    Chemical Structure

    C6H6O2

    Each gram of MELAMIN-C™ (Hydroquinone USP, 4%) Skin Bleaching & Correcting Crème with 20% Vitamin C contains Hydroquinone USP 40mg/gm in a base of ascorbic acid, ascorbyl palmitate, caprylic/capric triglyceride, caprylyl methicone, cetyl PEG/PPG-10/1 dimethicone, cyclotetrasiloxane, dimethicone, dimethicone crosspolymer, tocopheryl acetate, ethoxydiglycol, helianthus annuus (sunflower) seed oil, oleyl alcohol, pluenetia volubilis seed oil, retinyl palmitate, rosmarinus officinalis (rosemary) leaf extract, squalene, tocopherol, zanthoxylum bungeanum fruit extract.

  • CLINICAL PHARMACOLOGY

    Topical application of hydroquinone produces a reversible depigmentation of the skin by inhibition of the enzymatic oxidation of tyrosine to 3,4-dihydroxyphenylalanine (DOPA) and suppression of other melanocyte metabolic processes. Exposure to sunlight or ultraviolet light will cause re-pigmentation of bleached areas, which may be prevented by the use of the sunscreen agents.

  • INDICATIONS AND USAGE

    For the gradual bleaching of hyperpigmented skin conditions such as cholasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation.

  • CONTRAINDICATIONS

    Prior history of sensitivity or allergic reaction to hydroquinone or to any other ingredient in this product. The safety of topical hydroquinone use during pregnancy or in children (21 years and under) has not been established.

  • WARNINGS

    Hydroquinone is a skin bleaching agent which may produce undesired effects if not used as directed. The physician should be familiar with the contents of this insert before prescribing or dispensing this product.

    Avoid unnecessary sun exposure, use an effective broad-spectrum sunscreen agent or protective clothing should be worn to cover bleached skin to prevent re-pigmentation from occurring.

    Hydroquinone may produce exogenous ochronosis, a gradual blue-black darkening of the skin. If his condition occurs, discontinue treatment and consult your physician.

    Avoid contact with eyes and mucous membranes. Keep out of reach of children. In case of accidental ingestion, call a physician or a poison control center immediately.

  • PRECAUTIONS

    Test for skin sensitivity before using by applying a small amount to an unbroken patch of skin; check within 24 hours. Minor redness is not a contraindication, but where there is itching or vesicle formation or excessive inflammatory response, further treatment is not advised. Close patient supervision is recommended.

    Drug Interactions

    Patients are cautioned on concomitant use of medications that are known to be photosensitizing.

    Carcinogenesis, Mutagenesis, Impairment of Fertility

    Studies of hydroquinone in animals have demonstrated some evidence of carcinogenicity. The carcinogenic potential of hydroquinone in humans is unknown.

    Pregnancy Category C

    Animal reproduction studies have not been conducted with topical hydroquinone. It is also not known whether topical hydroquinone can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Topical hydroquinone should be given to a pregnant woman only if clearly needed.

    Nursing Mothers

    It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when topical hydroquinone is administered to a nursing woman.

    Pediatric Use

    Safety and effectiveness for pediatric patients below the age of 12 years have not been established.

    Adverse Reactions

    The following reactions have been reported: dryness and fissuring of paranasal and infraorbital areas, erythema, and stinging. Occasional hypersensitivity (localized contact dermatitis) may develop. If this occurs, the medication should be discontinued, and the physician notified immediately.

    Overdosage

    There have been no system reactions reported from the use of topical hydroquinone. However, treatment should be limited to relatively small areas of the body at one time, since some patients experience a transient skin reddening and a mild burning sensation which does not preclude treatment.

  • DRUG DOSAGE AND ADMINISTRATION

    A thin layer of MELAMIN-C™ (Hydroquinone USP, 4%) Skin Bleaching & Correcting Crème with 20% vitamin C should be applied to the affected area twice daily or as directed by a physician. If no improvement is seen after 8-12 weeks of treatment, use of this product should be discontinued. There is no recommended dosage for pediatric patients under 12 years of age except under the advice and supervision of a physician.

  • HOW SUPPLIED

    MELAMIN-C™ (Hydroquinone USP, 4%) Skin Bleaching & Correcting Crème with 20% Vitamin C is available as follows:

    2.99 Oz. (85 g) Bottle / NDC 42851-034-85

    1.19 Oz. (34 g) Bottle / NDC 42851-034-34

    STORAGE

    Store at controlled room temperature: 15°-30°C (59°-86°F)

  • PRINCIPAL DISPLAY PANEL - 85 g Bottle Carton

    ZO®MEDICAL
    BY ZEIN OBAGI MD

    NDC 42851-034-85

    MELAMIN-C™
    Skin Bleaching &
    Correcting Crème
    with 20% Vitamin C

    Hydroquinone USP, 4%

    RX ONLY

    Net Wt. 85 g / 2.99 Oz.

    Principal Display Panel - 85 g Bottle Carton
  • INGREDIENTS AND APPEARANCE
    ZO MEDICAL MELAMIN-C SKIN BLEACHING AND CORRECTING WITH VITAMIN C HYDROQUINONE 
    hydroquinone cream
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:42851-034
    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
    Ascorbic Acid (UNII: PQ6CK8PD0R)  
    Ascorbyl Palmitate (UNII: QN83US2B0N)  
    Medium-Chain Triglycerides (UNII: C9H2L21V7U)  
    Caprylyl Trisiloxane (UNII: Q95M2P1KJL)  
    Cyclomethicone 4 (UNII: CZ227117JE)  
    Dimethicone (UNII: 92RU3N3Y1O)  
    Dimethicone Crosspolymer (450000 MPA.S AT 12% in Cyclopentasiloxane) (UNII: UF7620L1W6)  
    .Alpha.-Tocopherol Acetate, D- (UNII: A7E6112E4N)  
    Diethylene Glycol Monoethyl Ether (UNII: A1A1I8X02B)  
    Sunflower Oil (UNII: 3W1JG795YI)  
    Oleyl Alcohol (UNII: 172F2WN8DV)  
    Plukenetia Volubilis Seed Oil (UNII: 8ED72Z8J1Z)  
    Vitamin A Palmitate (UNII: 1D1K0N0VVC)  
    Rosemary (UNII: IJ67X351P9)  
    Squalane (UNII: GW89575KF9)  
    Tocopherol (UNII: R0ZB2556P8)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42851-034-851 in 1 CARTON06/01/2016
    185 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    2NDC:42851-034-341 in 1 CARTON06/01/2016
    234 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Export only06/01/2016
    Labeler - ZO Skin Health, Inc. (826468527)
    Establishment
    NameAddressID/FEIBusiness Operations
    G.S. COSMECEUTICAL USA, INC.017014734MANUFACTURE(42851-034)

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