Label: BONDIBOOST SCALP SERUM- salicylic acid scalp serum liquid

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

Drug Label Information

Updated April 30, 2024

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

  • ACTIVE INGREDIENT

    Active IngredientsPurpose
    Salicylic Acid 2.00%Anti- Dandruff

  • ASK DOCTOR

    Stop use and ask a doctor if:

    • Conditin worsens, or if symptoms persist for more than 7 days
    • symptoms clear up and occur again within a few days
  • ASK DOCTOR/PHARMACIST

  • DO NOT USE

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • PURPOSE

    Uses

    For relief of itching, irritation, redness, flaking and scaling assoicated with Dandruff.

  • QUESTIONS

    Questions? 1(877)-241-0459

  • STOP USE

    Stop use and ask as doctor if

    • condition worsens, or if symptoms persist for more than 7 days
    • symptoms clear up and occur again within a few days
  • WARNINGS

    Warnings

    • For external use only
    • Avoid contact with the eyes. If contact occurs, rinse eyes throroughly with water.
    • If condition worsens, or does not improve adter regular use of this product as directed, consult a doctor
  • INACTIVE INGREDIENT

    Water (Aqua, Eau), Glycerin, Propanediol, Pentylene Glycol, Caprylyl Glycol, Ethylhexylglycerin, Menthol, Aloe Barbadensis Leaf Juice, Niacinamide, Zinc Pyrithione, Caffeine, Mentha Piperita (Peppermint) Oil, Arnica Montana Flower Extract, Cucumis Sativus (cucumber) Fruit Extract, Chamomilla Recutita (Matricaria) Extract, Panthenol, Xanthan Gum, Hydrolyzed Jojoba Esters, Sorbitan Oleate Decylglucoside Crosspolymer, Sodium Hydroxide.

  • DOSAGE & ADMINISTRATION

  • INDICATIONS & USAGE

    Uses

    For Relef of itching, irritaion, redness, flaking and scaling associated with Dandruff.

  • PRINCIPAL DISPLAY PANEL

    serum

  • INGREDIENTS AND APPEARANCE
    BONDIBOOST SCALP SERUM 
    salicylic acid scalp serum liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84169-004
    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
    GLYCERIN (UNII: PDC6A3C0OX)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    MATRICARIA CHAMOMILLA WHOLE (UNII: G0R4UBI2ZZ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    HYDROLYZED JOJOBA ESTERS (ACID FORM) (UNII: UDR641JW8W)  
    CAFFEINE (UNII: 3G6A5W338E)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    MENTHOL (UNII: L7T10EIP3A)  
    CUCUMIS SATIVUS WHOLE (UNII: 50560UL2YV)  
    PYRITHIONE ZINC (UNII: R953O2RHZ5)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84169-004-01125 mL in 1 BOTTLE; Type 0: Not a Combination Product02/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM03202/15/2024
    Labeler - Bondi Boost US LLC (119222402)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dhaliwal Pharmaceuticals Laboratories, LLC116933772manufacture(84169-004)