Label: HEAD AND SHOULDERS DEEP MOISTURE- pyrithione zinc shampoo
- NDC Code(s): 69423-247-37, 69423-247-38, 69423-247-65
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 15, 2025
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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, glycol distearate, zinc carbonate, sodium chloride, cocamidopropyl betaine, fragrance, sodium xylenesulfonate, dimethicone, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, sodium laureth sulfate, persea gratissima (avocado) oil, methylchloroisothiazolinone, methylisothiazolinone
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 370 mL Bottle Label
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS DEEP MOISTURE
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-247 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 WATER (UNII: 059QF0KO0R) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) SODIUM LAURYL SULFATE (UNII: 368GB5141J) DIMETHICONE (UNII: 92RU3N3Y1O) GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM BENZOATE (UNII: OJ245FE5EU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) AVOCADO OIL (UNII: 6VNO72PFC1) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) ZINC CARBONATE (UNII: EQR32Y7H0M) MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-247-38 380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/2017 12/01/2024 2 NDC:69423-247-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/2017 07/01/2021 3 NDC:69423-247-37 370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/2022 10/01/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 12/01/2017 10/01/2026 Labeler - The Procter & Gamble Manufacturing Company (004238200)

