Label: GLOVERS DANDRUFF CONTROL MEDICINE, REGULAR- sulfur suspension

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

Drug Label Information

Updated October 21, 2023

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  • Active Ingredients:

    Sulfur, 2.5%

    Purpose

    Antidandruff

  • Uses:

    Controls scalp itching and flaking due to dandruff

  • Warnings:

    For External Use Only.

    When using this product

    • do not get into eyes. If contact occurs rinse eyes thoroughly with water.

    Stop use and consult a doctor if

    • if skin irritation develops or increases.
    • 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 at once.

  • Directions:

    • Shake well before using.
    • For best results, use at leats twice a week, or as directed  by a doctor.
    • Before shampooimg your hair, apply a small amount to the scalp in several areas. Rub in well. Wait 15 minutes to 1 hour Shampoo thoroughly
  • Inactive Ingredients:

    Mineral Oil (Paraffum Liquidum), Polysorbate-85, Disteardimonium Hectorite, Propylene Glycol, Benzyl Alcohol, Fragrance (Parfum).

  • Package Labeling Bottle

    Bottle

  • Package Labeling:

    Carton

  • INGREDIENTS AND APPEARANCE
    GLOVERS DANDRUFF CONTROL MEDICINE, REGULAR 
    sulfur suspension
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR25 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP)  
    POLYSORBATE 85 (UNII: A7F3N56197)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-007-001 in 1 CARTON09/24/2001
    181 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03209/24/2001
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-007)
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