Label: SULFUR 8 ORIGINAL ANTI-DANDRUFF HAIR AND SCALP CONDITIONER- sulfur ointment

  • NDC Code(s): 12022-017-00, 12022-017-01, 12022-017-02
  • Packager: J. Strickland & Co.
  • Category: HUMAN OTC DRUG LABEL

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Updated October 21, 2023

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  • Active Ingredient

    Sulfur, 2%

    Purpose

    Antidandruff

  • Use:

    Controls scalp itching and flaking due to dandruff

  • Warnings:

    For external use only

    When using this product

    • Avoid contact with eyes. If contact occurs, rinse eyes throughly with water.

    Stop use and ask a doctor if

    • condition worsens or does not improve after regular use.

    Keep out of reach of children

    If swallower, get medical help or call a poison control center at once.

  • Directions

    • Apply to the affected area 1-4 times daily, or as directed by a doctor.
  • Inactive Ingredients

    Petrolatum, Landin, Sorbitan Trioleate, Pclysorbate 81, Menthol, Mineral Oil, Fragrance, Amyl Cinnamal, Cinnamal, Citral, Citronellol, Geraniol, Limonene, Linalool

  • 12022-017-00

    017-00

  • 12022-017-01

    017-01

  • 12022-017-02

    017-02

  • INGREDIENTS AND APPEARANCE
    SULFUR 8 ORIGINAL ANTI-DANDRUFF HAIR AND SCALP CONDITIONER 
    sulfur ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-017
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    LANOLIN (UNII: 7EV65EAW6H)  
    SORBITAN TRIOLEATE (UNII: QE6F49RPJ1)  
    MENTHOL (UNII: L7T10EIP3A)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    .ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)  
    CINNAMALDEHYDE (UNII: SR60A3XG0F)  
    CITRAL (UNII: T7EU0O9VPP)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    GERANIOL (UNII: L837108USY)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-017-0057 g in 1 JAR; Type 0: Not a Combination Product12/01/1990
    2NDC:12022-017-01113 g in 1 JAR; Type 0: Not a Combination Product12/01/1990
    3NDC:12022-017-02205 g in 1 JAR; Type 0: Not a Combination Product12/01/1990
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03212/01/1990
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-017)
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