Label: BONDIBOOST SCALP SERUM- salicylic acid scalp serum liquid
- NDC Code(s): 84169-004-01
- Packager: Bondi Boost US LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 23, 2024
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- ACTIVE INGREDIENT
- ASK DOCTOR
- ASK DOCTOR/PHARMACIST
- DO NOT USE
- KEEP OUT OF REACH OF CHILDREN
- PURPOSE
- QUESTIONS
- STOP USE
- WARNINGS
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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
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INGREDIENTS AND APPEARANCE
BONDIBOOST SCALP SERUM
salicylic acid scalp serum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:84169-004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:84169-004-01 125 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/15/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 02/15/2024 Labeler - Bondi Boost US LLC (119222402) Establishment Name Address ID/FEI Business Operations Dhaliwal Pharmaceuticals Laboratories, LLC 116933772 manufacture(84169-004)