Label: AVEDA SCALP REMEDY DADRUFF- salicylic acid solution

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

Drug Label Information

Updated July 27, 2023

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  • Active Ingredient

    Salicylic Acid 2.0%

  • Purpose

    Anti-dandruff

  • USE

    helps eliminate flaking and irritation

  • 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 contact a Poison Control Center right away.

  • Directions

    ■ Apply to affected areas 2 to 4 times daily or as
    directed by a doctor. ■ Do not rinse out.

  • Inactive Ingredients

    Water\Aqua\Eau, Alcohol Denat., Betaine,
    Sodium Methyl Cocoyl Taurate, Lippia Sidoides (Oregano) Leaf Oil,
    Rosmarinus Officinalis (Rosemary) Leaf Extract,
    Echinacea Purpurea (Coneflower) Extract, Arctium
    Lappa (Burdock) Root Extract, Salvia Officinalis
    (Sage) Leaf Extract, Narcissus Tazetta Bulb Extract,
    Glycerin, Dimethicone PEG-8 Meadowfoamate,
    Hydroxyethylcellulose, Fragrance (Parfum), Eugenol,
    Linalool, Citral, Limonene, Sodium Citrate, Sodium
    Chloride <ILN45198>

  • Principal Display Panel

    AVEDA
    Scalp Remedy
    DANDRUFF SOLUTION
    helps eliminate flaking and irritation
    4.2 fl oz/oz liq/125 ml e PDP

  • INGREDIENTS AND APPEARANCE
    AVEDA SCALP REMEDY DADRUFF 
    salicylic acid solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57677-065
    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
    LIPPIA SIDOIDES LEAF OIL (UNII: M86P9S87MR)  
    CITRAL (UNII: T7EU0O9VPP)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    NARCISSUS TAZETTA BULB (UNII: K17762966S)  
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    ECHINACEA PURPUREA (UNII: QI7G114Y98)  
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
    SAGE (UNII: 065C5D077J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    EUGENOL (UNII: 3T8H1794QW)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    BETAINE (UNII: 3SCV180C9W)  
    SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)  
    ROSEMARY (UNII: IJ67X351P9)  
    DIMETHICONE PEG-8 MEADOWFOAMATE (UNII: 53UN5B8F4W)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57677-065-01125 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product12/06/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03212/06/202209/10/2024
    Labeler - Aveda Corporation (071352058)
    Registrant - Estee Lauder Companies Inc. (790802086)
    Establishment
    NameAddressID/FEIBusiness Operations
    Marietta Corporation dba Voyant Beauty010765394manufacture(57677-065)
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