Label: BHS BEAUTIFUL HAIR AND SCALP- damage repair anti-dandruff conditioner liquid

  • NDC Code(s): 64942-1970-1
  • Packager: Conopco, Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 23, 2022

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  • BHS. BEAUTIFUL HAIR & SCALP DAMAGE REPAIR ANTI-DANDRUFF CONDITIONER - salicylic acid liquid

  • Drug Facts

    Active ingredient

    Salicylic Acid (2.0%)

  • Purpose

    Anti-dandruff

  • Use

    Helps prevent and control recurrence of itching, flaking and irritation associated with dandruff.

  • Warnings

    For external use only
    When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughtly 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

    Keep this and all drugs out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    For best results use at least twice per week or as directed by a doctor. Shake well, then massage into scalp and hair. Rinse.

  • Inactive Ingredients

    Water (Aqua), Cetearyl Alcohol, Stearamidopropyl Dimethylamine, Dimethiconol/Silsesquioxane Copolymer, Behentrimonium Chloride, Hydrolyzed Keratin, Gluconolactone, Isohexadecane, Fragrance (Parfum), Dipropylene Glycol, Sodium Benzoate, Disodium EDTA, Cetrimonium Chloride, Limonene, Linalool.

  • Questions or comments?

    Call 1-800-671-3998

  • Packaging

    bhs Damage Repair Anti-dandruff CD

  • INGREDIENTS AND APPEARANCE
    BHS BEAUTIFUL HAIR AND SCALP 
    damage repair anti-dandruff conditioner liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1970
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1970-1400 mL in 1 BOTTLE; Type 0: Not a Combination Product11/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H11/01/2021
    Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)
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