Home > Drugs A-Z > ELASTIDERM DECOLLETAGE SKIN LIGHTENING COMPLEX

ELASTIDERM DECOLLETAGE SKIN LIGHTENING COMPLEX (OMP, INC.)

Available Formats

Dosage Form Package Information Links
LOTION 1 TUBE in 1 CARTON (62032-120-60) > 57 g in 1 TUBE Label Information

Complete ELASTIDERM DECOLLETAGE SKIN LIGHTENING COMPLEX Information

  • SPL UNCLASSIFIED SECTION

    Rx Only
    FOR EXTERNAL USE ONLY

    Each gram of Skin Lightening Complex contains:


  • SPL UNCLASSIFIED SECTION

    Active ingredient:Hydroquinone USP, 4% (40 mg/g)

    Inactive ingredients: water, glycerin, cetyl alcohol, PPG-2 myristyl ether propionate, sodium lauryl sulfate, TEA-salicylate, lactic acid, phenyl trimethicone, tocopheryl acetate, sodium metabisulfite, ascorbic acid, methylparaben, disodium EDTA, propylparaben, saponins, BHT


  • Description:

    Hydroquinone is 1,4-benzenediol. The drug is freely soluble in water and in alcohol. Chemically, hydroquinone is designated as p-dihydroxybenzene; the empirical formula is C6H6O2; the molecular weight is 110.11 g/mol. The chemical structure is in the diagram to the right.

    Chemical Structure

  • 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 repigmentation of the bleached areas, which may be prevented by the use of sunblocking agents or sunscreen agents.


  • Indications and Usage:

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


  • Contraindications:

    People with prior history of sensitivity or allergic reaction to this product or any of its ingredients should not use it. The safety of topical hydroquinone use during pregnancy or in children (12 years and under) has not been established.


  • Dosage and Administration:

    A thin application should be applied once or twice daily or as directed by a physician. If no improvement is seen after three (3) months of treatment, use of this product should be discontinued. Sun exposure should be limited by using a sunscreen agent, a sunblocking agent, or protective clothing to cover bleached skin when using and after using this product in order to prevent darkening from reoccurring.


  • Warnings:

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

    Test for skin sensitivity before using by applying a small amount to an unbroken patch of skin and check within 24 hours. Minor redness is not a contraindication, but where there is itching or vesicle formation or excessive inflammatory response, the product should be discontinued and a physician consulted. Close patient supervision is recommended.

    Avoid contact with the eyes, nose, mouth, and lips. In case of accidental contact, the patient should rinse thoroughly with water and contact a physician.

    Sunscreen use is an essential aspect of hydroquinone therapy because even minimal sunlight exposure sustains melanocytic activity.

    Contains sodium metabisulfite, a sulfite that may cause allergic-type reactions including anaphylactic symptoms and life-threatening or less severe asthmatic episodes in certain susceptible people. The overall prevalence of sulfite sensitivity in the general population is unknown and probably low. Sulfite sensitivity is seen more frequently in asthmatic than in nonasthmatic people.


  • Precautions:

    (also see WARNINGS)

    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.

    Pregnancy Category C:

    Animal reproduction studies have not been conducted with topical hydroquinone. It is also not known whether hydroquinone can cause fetal harm when used topically on a pregnant woman or affect reproductive capacity. It is not known to what degree, if any, topical hydroquinone is absorbed systemically. Topical hydroquinone should be used on pregnant women only when clearly indicated.

    Nursing Mothers:

    It is not known whether topical hydroquinone is absorbed or excreted in human milk. Caution is advised when topical hydroquinone is used by a nursing mother.

    Pediatric Usage:

    Safety and effectiveness in children below the age of 12 years have not been established.


  • Adverse Reactions:

    No systemic adverse reactions have been reported. Occasional hypersensitivity (localized contact dermatitis) may occur, in which case the product should be discontinued and the physician notified immediately.


  • How Supplied:

    Obagi Skin Lightening Complex is available as follows:

    2.0 oz. (57 g) tube
    NDC 62032-120-60

    Store at controlled room temperature:
    15°C-25°C (59°F-77°F)


  • SPL UNCLASSIFIED SECTION

    OBAGI®
    MEDICAL

    Obagi is a registered trademark of OMP, Inc.
    Distributed by OMP, Inc.
    © 2012 Obagi Medical Products, Inc.

    All rights reserved.
    Long Beach, CA 90806
    Made in USA. www.obagi.com
    60650612Z 09/12


  • PRINCIPAL DISPLAY PANEL - 57 g Carton

    NDC 62032-120-60

    OBAGI®
    MEDICAL

    ELASTIderm®
    décolletage

    Chest and Neck

    Skin Lightening Complex

    Hydroquinone USP, 4%
    Rx Only

    Net wt. 2 oz. (57 g)

    Obagi Decolletage Skin Lightening Complex Carton

  • INGREDIENTS AND APPEARANCE
    ELASTIDERM DECOLLETAGE SKIN LIGHTENING COMPLEX  CHEST AND NECK
    hydroquinone lotion
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:62032-120
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE 40 mg  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PPG-2 MYRISTYL ETHER PROPIONATE (UNII: 88R97D8U8A)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    TROLAMINE SALICYLATE (UNII: H8O4040BHD)  
    LACTIC ACID (UNII: 33X04XA5AT)  
    PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    Product Characteristics
    Color GRAY Score     
    Shape Size
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:62032-120-60 1 in 1 CARTON
    1 57 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    Unapproved drug other 12/01/2010
    Labeler - OMP, INC. (790553353)
    Establishment
    Name Address ID/FEI Business Operations
    PureTek Corporation 785961046 MANUFACTURE(62032-120) , LABEL(62032-120) , PACK(62032-120)