Label: SULFUR 8 MEDICATED DANDRUFF WITH SALICYLIC ACID- salicylic acid liquid

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

Drug Label Information

Updated November 5, 2023

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  • Drug Facts

  • Active Ingredient

    Salicylic Acid, 2%

    Purpose

    Antidandruff, Seborrheic dermatitis, Psoriasis.

  • Uses

    control the symptoms of 

    • dandruff 
    • seborrheic dermatitis
    • psoriasis
  • Warnings

    For external use only

    Ask a doctor before use 

    if you have 

    • a condition that covers a large area of the body.

    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.

  • Directions

    • For best results, use at least twice a week or as directed by a doctor. 
    • Apply a liberal amount of shampoo and massage into lather.
    • Allow lather to remain on scalp for a few minutes.
    • Rinse and repeat.
  • Inactive Ingrdients

    Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Sodium Chloride, Polyquaternium-22, Menthol, Aloe Barbadensis Leaf Extract, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Disodium EDTA, Sodium Benzoate, Citric Acid, Potassium Sorbate, Sodium Sulfite, Sodium Hydroxide, Benzyl Benzoate, Fragrance.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    SULFUR 8 MEDICATED DANDRUFF WITH SALICYLIC ACID 
    salicylic acid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-039
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    MENTHOL (UNII: L7T10EIP3A)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    SODIUM SULFITE (UNII: VTK01UQK3G)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    BENZYL BENZOATE (UNII: N863NB338G)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-039-00222 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03210/01/2023
    Labeler - J. Strickland and Co. (007023112)
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