Label: RE-FRESH SCALP CARE- salicylic acid liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 64942-1638-1 - Packager: Conopco, Inc. d/b/a/ Unilever
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 7, 2022
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- RE-FRESH SCALP CARE EUCALYPTUS + COOLING RELIEF ANTI-DANDRUFF CONDITIONER - salicylic acid liquid
- Drug Facts
- Purpose
- Use
- Warnings
- KEEP OUT OF REACH OF CHILDREN
- Directions
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Inactive Ingredients
Water (Aqua), Cetearyl Alcohol, Stearamidopropyl Dimethylamine, Behentrimonium Chloride, Cocos Nucifera (Coconut) Oil, Menthol, Eucalyptus Globulus Leaf Oil, Salix Alba (Willow) Bark Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Arctium Lappa Root Extract, Ginkgo Biloba Leaf Extract, Salvia Officinalis (Sage) Leaf Extract, Hippophae Rhamnoides Fruit Extract, Propylene Glycol, Fragrance (Parfum), Sodium Benzoate, Dipropylene Glycol, Disodium EDTA, Benzyl Salicylate. Citral, Hexyl Cinnamal, Limonene, Linalool.
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INGREDIENTS AND APPEARANCE
RE-FRESH SCALP CARE
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:64942-1638 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 2 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) STEARAMIDOPROPYL DIMETHYLAMINE (UNII: K7VEI00UFR) BEHENTRIMONIUM CHLORIDE (UNII: X7GNG3S47T) COCONUT OIL (UNII: Q9L0O73W7L) MENTHOL (UNII: L7T10EIP3A) EUCALYPTUS OIL (UNII: 2R04ONI662) ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3) GINKGO (UNII: 19FUJ2C58T) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SODIUM BENZOATE (UNII: OJ245FE5EU) DIPROPYLENE GLYCOL (UNII: E107L85C40) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) BENZYL SALICYLATE (UNII: WAO5MNK9TU) CITRAL (UNII: T7EU0O9VPP) .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I) LIMONENE, (+)- (UNII: GFD7C86Q1W) LINALOOL, (+/-)- (UNII: D81QY6I88E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:64942-1638-1 400 mL in 1 CONTAINER; Type 0: Not a Combination Product 05/10/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 05/10/2019 Labeler - Conopco, Inc. d/b/a/ Unilever (001375088)