Label: BRICKELL MENS PRODUCTS RELIEVING ANTI-DANDRUFF- salicylic acid liquid
- NDC Code(s): 82247-617-00
- Packager: BRICKELL BRANDS LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 16, 2025
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- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Uses
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Warnings
For external use only
Use caution in exposing skin to sunlight after applying this product. It may increase your tendency to sunburn for up to 24 hours after application.
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
- Directions
- Other Information
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Inactive Ingredients
Aloe Barbadensis Leaf Juice, Citrus Limon (Lemon) Fruit Extract, Cocamidopropyl Betaine, Decyl Glucoside, Glycerin, Guar Hydroxypropyltrimonium Chloride, Hydrolyzed Quinoa, Lactic Acid, Lamium Album Extract, Lauramine Oxide, Lavandula Angustifolia (Lavender) Flower Oil, Nelumbo Nucifera Flower Extract, Panthenol, Phenoxyethanol, Propanediol, Resveratrol, Ricinus Communis (Castor) Seed Oil, Rosa Canina Fruit Oil, Salix Alba (Willow) Bark Extract, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium C14-16 Olefin Sulfonate, Sodium Hydroxide, Symphytum Officinale Extract, Tetrasodium Glutamate Diacetate, Tocopherol, Water (Aqua), Xanthan Gum, Ziziphus Joazeiro Bark Extract, Mentha Piperita (Peppermint) Essential Oil, Melaleuca Alternifolia (Tee Tree) Leaf Essential Oil
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- Package Labeling:
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INGREDIENTS AND APPEARANCE
BRICKELL MENS PRODUCTS RELIEVING ANTI-DANDRUFF
salicylic acid liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:82247-617 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID 18 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB) LEMON BALM OIL (UNII: MJ76269K9S) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) DECYL GLUCOSIDE (UNII: Z17H97EA6Y) GLYCERIN (UNII: PDC6A3C0OX) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (UNII: B16G315W7A) LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT) LAMIUM ALBUM WHOLE (UNII: 046Y1357I6) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) NELUMBO NUCIFERA FLOWER (UNII: 61W322NLDV) PANTHENOL (UNII: WV9CM0O67Z) PHENOXYETHANOL (UNII: HIE492ZZ3T) PROPANEDIOL (UNII: 5965N8W85T) RESVERATROL (UNII: Q369O8926L) CASTOR OIL (UNII: D5340Y2I9G) ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ) SALIX ALBA BARK (UNII: 205MXS71H7) JOJOBA OIL (UNII: 724GKU717M) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) SODIUM HYDROXIDE (UNII: 55X04QC32I) TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY) TOCOPHEROL (UNII: R0ZB2556P8) WATER (UNII: 059QF0KO0R) XANTHAN GUM (UNII: TTV12P4NEE) SARCOMPHALUS JOAZEIRO BARK (UNII: 4ZYT6RK5T9) PEPPERMINT (UNII: V95R5KMY2B) MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82247-617-00 237 mL in 1 BOTTLE; Type 0: Not a Combination Product 05/28/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 05/28/2025 Labeler - BRICKELL BRANDS LLC (081141606) Registrant - Pure Source, LLC (080354456) Establishment Name Address ID/FEI Business Operations Pure Source, LLC 080354456 manufacture(82247-617)

