Label: SULFUR 8 FRESH ANTI-DANDRUFF HAIR AND SCALP CONDITIONER- salicylic acid ointment

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

Drug Label Information

Updated October 21, 2023

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  • Active Ingredients

    Salicylic Acid, 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

    Keep out of reach of children

    If swallowed, 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, Cetyl Alcohol, Paraffin, Butyrospermum Parkii (Shea Butter), Theobromo Grandiflorum Seed Butter, Mineral Oil, Menthol, Fragrance, Sorbitan Trioleate, Allantion, Polysorbate 81

  • Package Labeling:

    022-026

  • INGREDIENTS AND APPEARANCE
    SULFUR 8 FRESH ANTI-DANDRUFF HAIR AND SCALP CONDITIONER 
    salicylic acid ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-026
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    PETROLATUM (UNII: 4T6H12BN9U)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    MENTHOL (UNII: L7T10EIP3A)  
    SORBITAN TRIOLEATE (UNII: QE6F49RPJ1)  
    ALLANTOIN (UNII: 344S277G0Z)  
    POLYSORBATE 81 (UNII: 2MSF640LWM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:12022-026-00108 g in 1 JAR; Type 0: Not a Combination Product02/06/2008
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03202/06/2008
    Labeler - J. Strickland & Co. (007023112)
    Registrant - J. Strickland & Co. (007023112)
    Establishment
    NameAddressID/FEIBusiness Operations
    J. Strickland & Co.007023112manufacture(12022-026)
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