Label: HEAD AND SHOULDERS SUPREME DETOXIFYING PRE-WASH MASK- pyrithione zinc cream
- NDC Code(s): 69423-407-50
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated July 6, 2023
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Inactive ingredients
Water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, zinc carbonate, sodium chloride, sodium xylenesulfonate, fragrance, argania spinosa kernel oil, tocopheryl acetate, cocamidopropyl betaine, dimethicone, menthol, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, mentha piperita (peppermint) oil, mentha arvensis leaf oil, eucalyptus globulus leaf extract, methylchloroisothiazolinone, methylisothiazolinone.
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- PRINCIPAL DISPLAY PANEL - 50 mL pouch Label
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS SUPREME DETOXIFYING PRE-WASH MASK
pyrithione zinc creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-407 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 1 g in 100 mL Inactive Ingredients Ingredient Name Strength SODIUM LAURYL SULFATE (UNII: 368GB5141J) PEPPERMINT OIL (UNII: AV092KU4JH) MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N) EUCALYPTUS OIL (UNII: 2R04ONI662) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4) ZINC CARBONATE (UNII: EQR32Y7H0M) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) ARGAN OIL (UNII: 4V59G5UW9X) GLYCOL DISTEARATE (UNII: 13W7MDN21W) ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) SODIUM BENZOATE (UNII: OJ245FE5EU) WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-407-50 50 mL in 1 POUCH; Type 0: Not a Combination Product 11/21/2019 09/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M032 11/21/2019 09/01/2024 Labeler - The Procter & Gamble Manufacturing Company (004238200)