Label: HEAD AND SHOULDERS MEN ADVANCED SERIES REFRESHING 2IN1 MENTHOL- pyrithione zinc lotion/shampoo
- NDC Code(s): 69423-312-37, 69423-312-38, 69423-312-65
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated March 31, 2023
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
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Inactive ingredients
Water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, sodium chloride, zinc carbonate, dimethicone, cocamidopropyl
betaine, sodium xylenesulfonate, fragrance, menthol, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide,mentha piperita (peppermint) flower/leaf/stemoil, mentha arvensis leaf/stem oil, blue 1, red 33 - Questions (or comments)?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 370 mL Bottle Label
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS MEN ADVANCED SERIES REFRESHING 2IN1 MENTHOL
pyrithione zinc lotion/shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-312 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 FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) MENTHOL (UNII: L7T10EIP3A) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N) PEPPERMINT OIL (UNII: AV092KU4JH) WATER (UNII: 059QF0KO0R) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) GLYCOL DISTEARATE (UNII: 13W7MDN21W) ZINC CARBONATE (UNII: EQR32Y7H0M) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM BENZOATE (UNII: OJ245FE5EU) MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4) MENTHA PIPERITA LEAF (UNII: A389O33LX6) SODIUM LAURYL SULFATE (UNII: 368GB5141J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-312-38 380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 12/15/2024 2 NDC:69423-312-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 12/01/2022 3 NDC:69423-312-37 370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/15/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M032 11/29/2018 Labeler - The Procter & Gamble Manufacturing Company (004238200)