Label: GLOVERS MEDICATED ANTI-DANDRUFF- coal tar shampoo

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated October 21, 2023

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  • Active Ingredients

    Coal Tar Solution, 2.5%

    Purpose

    Antidandruff, Antipsoriasis (Equivalent to Coal Tar USP, 0.5%)

  • Uses:

    Controls scalp itching and flaking due to dandruff

  • Warnings:

    For external use only

    Ask A doctor before use

    • if the condition covers a large area of your body
    • with other forms of psoriasis therapy such as prescription drugs or UV radition

    When using this product

    • Do not get into eyse. If contact occurs, rinse eyes thoroughly with water
    • Use caution in exposing the skin to sunlight after using this product. It may increase your tendency to sunburn for up to 24 hours after application.

    Stop use and consult a doctor if

    • condition worsens or does not improve after regular use.

    Keep out of reach of children.

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

  • Directions

    • Wet hair, apply to scalp and massage. Rinse and repeat.
    • For best results, use at least twice a week.
  • Inactive Ingredients

    Water, Ammonium Lauryl Sulfate, Ammonium Laureth Sufate, Polysorbate-20, Potassiuym Cocoyl Hydrolyzed Collagen, Cocamidopropyl Betaine, PEG-3 Glyceryl Cocoate, Fragrance, Benzyl Alcohol, Methylchloroisothiazolinone, Methylisothiazolinone, Triethylene Glycol, Propylene Glycol, Magnesium Nitrate, Magnesium Chloride, Citric Acid.

  • Package Labeling

    12022-010-00

  • INGREDIENTS AND APPEARANCE
    GLOVERS MEDICATED ANTI-DANDRUFF 
    coal tar shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-010
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    COAL TAR (UNII: R533ESO2EC) (COAL TAR - UNII:R533ESO2EC) COAL TAR25 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    TRIETHYLENE GLYCOL (UNII: 3P5SU53360)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-010-00118 mL in 1 BOTTLE; Type 0: Not a Combination Product10/31/2001
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03210/31/2001
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-010)
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