Label: GLOVERS DANDRUFF CONTROL MED., FLORAL- sulfur suspension

  • 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 October 13, 2022

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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.

    Flammable

    Keep away from heat and open flame

  • 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

    Carton

  • INGREDIENTS AND APPEARANCE
    GLOVERS DANDRUFF CONTROL MED., FLORAL 
    sulfur suspension
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-008
    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:12022-008-001 in 1 CARTON11/05/2001
    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 finalpart358H11/05/2001
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-008)
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