Label: BHS BEAUTIFUL HAIR AND SCALP- fresh detox 2 in 1 anti-dandruff shampoo shampoo

  • NDC Code(s): 64942-1973-1
  • Packager: Conopco, Inc. d/b/a/ Unilever
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 7, 2024

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  • BHS. BEAUTIFUL HAIR & SCALP FRESH DETOX 2 IN 1 ANTI-DANDRUFF SHAMPOO - salicylic acid liquid

  • Drug Facts

    Active ingredient

    Salicylic Acid (3.0%)

  • 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), Cocamidopropyl Betaine, Sodium C14-16 Olefin Sulfonate, Sodium Chloride, Charcoal Powder, Menthol, Disodium Laureth Sulfosuccinate, Polysorbate 80, Fragrance (Parfum), Phenoxyethanol, PEG-150 Pentaerythrityl Tetrastearate, Sodium Lauryl Sulfoacetate, PPG-2 Hydroxyethyl Cocamide, Guar Hydroxypropyltrimonium Chloride, Sodium Sulfate, Chlorphenesin, Silicone Quaternium-22, Tetrasodium EDTA, Dipropylene Glycol, Polyglyceryl-3 Caprate, PEG/PPG-18/18 Dimethicone, Phenol, Limonene, Linalool.

  • Questions or comments?

    Call 1-800-671-3998

  • Packaging

    bhs Fresh Detox Anti-dandruff SH

  • INGREDIENTS AND APPEARANCE
    BHS BEAUTIFUL HAIR AND SCALP 
    fresh detox 2 in 1 anti-dandruff shampoo shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-1973
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID3 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    PHENOL (UNII: 339NCG44TV)  
    MENTHOL (UNII: L7T10EIP3A)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYGLYCERYL-3 CAPRATE (UNII: VZQ347QQ3H)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    DISODIUM LAURETH SULFOSUCCINATE (UNII: D6DH1DTN7E)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    PEG-150 PENTAERYTHRITYL TETRASTEARATE (UNII: 8L4OOQ76AM)  
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
    SODIUM LAURYL SULFOACETATE (UNII: D0Y70F2B9J)  
    PPG-2 HYDROXYETHYL COCAMIDE (UNII: 34N07GUJ3X)  
    GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-1973-1400 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 DrugM03211/01/2021
    Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)
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