Label: OUAI ANTI-DANDRUFF- salicylic acid shampoo

  • NDC Code(s): 83058-0140-1, 83058-0140-4
  • Packager: United Beauty Brands, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 11, 2024

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Salicylic Acid 2%

  • Purpose

    Anti-Dandruff

  • Use

    Reduces scalp flaking, itching, and irritation associated with dandruff

  • Warnings

    For external use only

    When using this product avoid contact with the 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 of this product as directed.

    Keep out of reach of children. If swallowed, get medical help or contact a poison control right away.

  • Directions

    • Apply to wet hair and massage into scalp.
    • Leave on for 5 minutes and rinse thoroughly.
    • For best results use at least twice a week or as directed by a doctor.
  • Inactive Ingredients

    Water, Cocamidopropyl Betaine, Sodium C14-16 Olefin Sulfonate, Glycerin, Sodium Lauroyl Methyl Isethionate, Polysorbate 80, Acrylates Copolymer, Propanediol Caprylate, Potassium Hydroxide, Sodium Benzoate, Sodium Methyl Oleoyl Taurate, Sodium Cocoyl Isethionate, Cocamide MIPA, Cassia Hydroxypropyltrimonium Chloride, Polyquaternium-113, Chlorphenesin, Tetrasodium EDTA, Silicone Quaternium-22, Dipropylene Glycol, Epilobium Angustifolium Flower/Leaf/Stem Extract, Polyglyceryl-3 Caprate, PEG-45M, Citric Acid, Fragrance.

  • Questions or comments

    team@theouai.com

  • SPL UNCLASSIFIED SECTION

    DIST. BY OUAI BEVERLY HILLS,
    CA 90210 USA

  • PRINCIPAL DISPLAY PANEL - 300 ml Bottle Label

    OUAI

    ANTI-DANDRUFF SHAMPOO

    2% SALICYLIC ACID

    10 fl oz / 300 ml

    PRINCIPAL DISPLAY PANEL - 300 ml Bottle Label
  • INGREDIENTS AND APPEARANCE
    OUAI ANTI-DANDRUFF 
    salicylic acid shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83058-0140
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Salicylic Acid (UNII: O414PZ4LPZ) (Salicylic Acid - UNII:O414PZ4LPZ) Salicylic Acid2 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    Cocamidopropyl Betaine (UNII: 5OCF3O11KX)  
    Sodium C14-16 Olefin Sulfonate (UNII: O9W3D3YF5U)  
    Glycerin (UNII: PDC6A3C0OX)  
    Sodium Lauroyl Methyl Isethionate (UNII: II6VCD3S6R)  
    Polysorbate 80 (UNII: 6OZP39ZG8H)  
    Acrylates Crosspolymer-4 (UNII: GEV2EL4D9G)  
    Propanediol Caprylate (UNII: 7641PCH336)  
    Potassium Hydroxide (UNII: WZH3C48M4T)  
    Sodium Benzoate (UNII: OJ245FE5EU)  
    Sodium Methyl Oleoyl Taurate (UNII: 8PZ076134H)  
    Sodium Cocoyl Isethionate (UNII: 518XTE8493)  
    COCO MONOISOPROPANOLAMIDE (UNII: 21X4Y0VTB1)  
    Chlorphenesin (UNII: I670DAL4SZ)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Dipropylene Glycol (UNII: E107L85C40)  
    EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)  
    Polyglyceryl-3 Caprate (UNII: VZQ347QQ3H)  
    POLYETHYLENE OXIDE 2000000 (UNII: 5K3991GVWI)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83058-0140-1300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/17/2022
    2NDC:83058-0140-430 mL in 1 TUBE; Type 0: Not a Combination Product11/17/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM03211/17/2022
    Labeler - United Beauty Brands, LLC (080321665)