Label: GLOVERS ANTI-DANDRUFF- sulfur, salicylic acid ointment

  • NDC Code(s): 12022-009-00, 12022-009-01
  • Packager: J. Strickland & Co.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 21, 2023

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  • Active ingredients

    Sulfur, 5%

    Salicylic Acid, 3%

    Purpose

    Antidandruff

    Antidandruff

  • Uses

    • relieves the itching and scaling associated with dandruff
  • Warnings

    For external use only

    When using this product

    • Do not get in eyes. If contact occurs, rinse eyes thoroughly with water

    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

    Apply a small amount to the scalp one to four times daily or as directed by a doctor

  • Inactive Ingredients

    Petrolatum, Mineral Oil, Glyceryl Tribehenate, Arachidyl Propionate, Fragrance, Polysorbate-20, Propylparaben, Iron Oxides, Talc.

  • Package Labeling

    12022-009-00

  • Package Labeling

    12022-009-01

  • INGREDIENTS AND APPEARANCE
    GLOVERS ANTI-DANDRUFF 
    sulfur, salicylic acid ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR50 mg  in 1 g
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID30 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    TRIBEHENIN (UNII: 8OC9U7TQZ0)  
    ARACHIDYL PROPIONATE (UNII: QV5DAH3MSB)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    TALC (UNII: 7SEV7J4R1U)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-009-0028 g in 1 JAR; Type 0: Not a Combination Product09/20/2001
    2NDC:12022-009-0199 g in 1 JAR; Type 0: Not a Combination Product09/20/2001
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03209/20/2001
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-009)
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