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

  • NDC Code(s): 12022-018-00, 12022-018-01, 12022-018-02
  • 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, 2%

    Purpose

    Antidandruff

  • Use:

    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 ask a doctor if

    • condition worsens or does not improve after regular use.

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

    • a gradual blue-black darking of the skin occurs
    • irritation becomes severe
    • no improvement is seen after 3 months
  • Directions

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

    Petrolatum, Lanolin, Mineral Oil, Menthol, Fragrance, Yellow 11.

  • 12022-018-00

    018-00

  • 12022-018-01

    018-01

  • 12022-018-02

    018-02

  • INGREDIENTS AND APPEARANCE
    SULFUR 8 LIGHT ANTI-DANDRUFF HAIR AND SCALP CONDITIONER 
    sulfur ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-018
    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)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    MENTHOL (UNII: L7T10EIP3A)  
    D&C YELLOW NO. 11 (UNII: 44F3HYL954)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-018-0057 g in 1 JAR; Type 0: Not a Combination Product12/01/1990
    2NDC:12022-018-01113 g in 1 JAR; Type 0: Not a Combination Product12/01/1990
    3NDC:12022-018-02205 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(12022-018)
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