Label: GLOVERS MEDICATED ANTI-DANDRUFF SCALP- salicylic acid solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 21, 2023

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  • Active Ingredient

    Salicylic Acid, 3%

    Purposes

    Antidandruff,

    Seborrheic Dermatitis,

    Psoriasis

  • Use

    for relief of scalp itching, irritation, redness, scaling and flaking associated with dandruff, seborrheic dermatitis and psoriasis.

  • Warnings:

    For External Use Only.

    Ask a doctor before use if

    the condition covers a large area of the body

    When using this product

    • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

    Stop use and ask a doctor if

    condition worsens or does not improve after regular use of this product as directed.

    Keep out of reach of children

    If swallowed, get medical help or call a poison control center right away.

    Flammable

    Keep away from heat and open flame.

  • Directions:

    • Apply to the affected area one to four times daily or as directed by a doctor
    • Use after shampooing or between shampoos.

  • Inactive Ingredients:

    SD Alcohol 40, Water, Propylene Glycol, Benzyl Alcohol, Menthol.

  • PRINCIPAL DISPLAY PANEL

    011-00011-01

  • INGREDIENTS AND APPEARANCE
    GLOVERS MEDICATED ANTI-DANDRUFF SCALP 
    salicylic acid solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-011-001 in 1 CARTON11/05/2001
    175 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03211/05/2001
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-011)
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