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
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 14, 2018

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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

    12022-009-00 1

  • Package Labeling 12022-009-01

    12022-009-01 2

  • 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 finalpart358H09/20/2001
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-009) , pack(12022-009) , label(12022-009)
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