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Scarlight MD (Scarguard Labs, LLC)

Available Formats

Dosage Form Package Information Links
LIQUID 30 mL in 1 BOTTLE, WITH APPLICATOR (64269-9902-8) Label Information
LIQUID 15 mL in 1 BOTTLE, WITH APPLICATOR (64269-9902-7) Label Information

Complete Scarlight MD Information

  • Active Ingredients

    Hydroquinone 2%

  • Purpose

    Skin Lightener

  • Uses

    • lightens dark (brownish) discoloration in the skin such as age and liver spots

  • Warnings

    For external use only

  • Do not use

    • on children under 12 years of age.  Consult a doctor.
    • on mucous membranes

  • When using this product

    • mild irritation may occur
    • avoid contact with eyes.  If contact occurs, rinse with water.

  • Stop use and ask a doctor if

    • irritation becomes severe
    • condition worsens

  • Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • adults: brush a small amount twice daily. Rub in.
    • limit sun exposure and use a sunscreen, a sun blocking agent or protective clothing to cover bleached skin when using and after using this product in order to prevent darkening from reoccurring
    • discontinue if symptoms persist for more than 3 months
    • children under 12 years of age, consult a doctor before use

  • Other Information

    • store at 15º to 30ºC (59 to 86ºF)
    • keep bottle tightly closed or product will evaporate

  • Inactive Ingredients

    retinoic acid, melatonin, MSM, BHT, na metabisulfite, arbutin, cystamine, licorice root, dandelion root, hydroxyanisole, ascorbic acid, hydroxypropylcellulose, kojic acid, azelaic acid, acetone, propylene glycol, ethyl alcohol (SDA), distilled water q.s.

  • Questions


  • Carton 15mL

    15mL Label

  • Carton 30mL

    30mL Label

    hydroquinone liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:64269-9902
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    HYDROQUINONE (UNII: XV74C1N1AE) (Hydroquinone - UNII:XV74C1N1AE) HYDROQUINONE 20 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    Propylene Glycol (UNII: 6DC9Q167V3)  
    Alcohol (UNII: 3K9958V90M)  
    Acetone (UNII: 1364PS73AF)  
    Azelaic Acid (UNII: F2VW3D43YT)  
    Hydroxypropyl Cellulose (UNII: RFW2ET671P)  
    Ascorbic Acid (UNII: PQ6CK8PD0R)  
    Butylated Hydroxyanisole (UNII: REK4960K2U)  
    Licorice (UNII: 61ZBX54883)  
    Arbutin (UNII: C5INA23HXF)  
    Sodium Metabisulfite (UNII: 4VON5FNS3C)  
    Butylated Hydroxytoluene (UNII: 1P9D0Z171K)  
    Dimethyl Sulfone (UNII: 9H4PO4Z4FT)  
    Melatonin (UNII: JL5DK93RCL)  
    Tretinoin (UNII: 5688UTC01R)  
    Water (UNII: 059QF0KO0R)  
    Kojic Acid (UNII: 6K23F1TT52)  
    Cystamine (UNII: R110LV8L02)  
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:64269-9902-8 30 mL in 1 BOTTLE, WITH APPLICATOR
    2 NDC:64269-9902-7 15 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part358 11/01/2002
    Labeler - Scarguard Labs, LLC (842204575)
    Registrant - Scarguard Labs, LLC (842204575)