Label: SULFUR 8 LOC TWIST AND BRAID SCALP- salicylic acid solution

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

Drug Label Information

Updated October 21, 2023

If you are a consumer or patient please visit this version.

  • Active Ingredients

    Salicylic Acid, 3%

    Purpose

    Antidandruff

  • Use:

    relieves scalp itching, irritation, redness, scaling and flaking associated with dandruff

  • Warnings:

    For external use only

    When using this product

    • avoid contact with 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 of this product as directed.

    Keep out of reach of children

    If swallowed, get medical help or call a poison control center right away.

    Flammable

    Keep away from heat and open flame.

  • Directions

    • Apply to the affected area one to four times daily or as directed by a doctor.
    • Use after shampooing or between shampoos
  • Inactive Ingredients

    SD Alcohol 40, Water, Propylene Glycol, Benzyl Alcohol, Menthol.

  • Package Labeling:

    025-00

  • INGREDIENTS AND APPEARANCE
    SULFUR 8 LOC TWIST AND BRAID SCALP 
    salicylic acid solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-025
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    MENTHOL (UNII: L7T10EIP3A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-025-0075 mL in 1 BOTTLE; Type 0: Not a Combination Product05/19/2003
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03205/19/2003
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-025)