Label: SHEA MOISTURE- apple cider vinegar anti-dandruff conditioner liquid

  • NDC Code(s): 64942-2083-1
  • 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 August 10, 2022

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  • SHEA MOISTURE APPLE CIDER VINEGAR ANTI-DANDRUFF CONDITIONER - salicylic acid liquid

  • Drug Facts

    Active ingredient

    Salicylic Acid (2%)

  • Purpose

    Anti-dandruff

  • Uses

    Helps prevent recurrence of flaking and itching 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 before use. Apply to wet hair, gently massage onto scalp and gently comb for even distribution. Leave on for three minutes, rinse and style as desired.

  • Inactive Ingredients

    Water, Cetearyl Alcohol, Cocos Nucifera (Coconut) Oil, Stearamidopropyl Dimethylamine, Behentrimonium Chloride, Glycerin, Butyrospermum Parkii (Shea) Butter, Acetic Acid, Niacinamide, Gluconolactone, Rosa Damascena Flower Extract, Centella Asiatica (Gotu Kola) Extract, Sodium Benzoate, Fragrance

  • Questions?

    Call us at 1-866-478-1925

  • Packaging

    Shea Butter Apple Cider Anti-dandruff CD

  • INGREDIENTS AND APPEARANCE
    SHEA MOISTURE 
    apple cider vinegar anti-dandruff conditioner liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64942-2083
    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)  
    STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    WATER (UNII: 059QF0KO0R)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    ACETIC ACID (UNII: Q40Q9N063P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    ROSA DAMASCENA FLOWER (UNII: JWB78P295A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:64942-2083-1384 mL in 1 BOTTLE; Type 0: Not a Combination Product12/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart358H12/01/2022
    Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)
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