Label: HEAD AND SHOULDERS COCONUT DAILY- pyrithione zinc shampoo
- NDC Code(s): 69423-315-25, 69423-315-37, 69423-315-40
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 16, 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 laureth sulfate, sodium lauryl sulfate, cocamidopropyl betaine, sodium xylenesulfonate, zinc carbonate, glycol distearate, fragrance, sodium chloride, dimethiconol, sodium benzoate, guar hydroxypropyltrimonium chloride, dimethicone, TEA-dodecylbenzenesulfonate, magnesium carbonate hydroxide, trideceth-10, zea mays (corn) silk extract, cocos nucifera (coconut) fruit extract, benzyl alcohol,methylchloroisothiazolinone,methylisothiazolinone, yellow 5, red 33, blue 1
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 370 mL Bottle Label
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS COCONUT DAILY
pyrithione zinc shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-315 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 METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) CORN SILK (UNII: 7D3VB244UX) D&C RED NO. 33 (UNII: 9DBA0SBB0L) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) COCONUT (UNII: 3RT3536DHY) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) WATER (UNII: 059QF0KO0R) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) DIMETHICONE (UNII: 92RU3N3Y1O) ZINC CARBONATE (UNII: EQR32Y7H0M) GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM BENZOATE (UNII: OJ245FE5EU) MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4) SODIUM LAURYL SULFATE (UNII: 368GB5141J) DIMETHICONOL GUM (UNII: 4MJ9GU3T1P) TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN) TRIDECETH-10 (UNII: G624N6MSBA) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) BENZYL ALCOHOL (UNII: LKG8494WBH) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-315-40 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 12/01/2024 2 NDC:69423-315-25 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 3 NDC:69423-315-37 370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 11/29/2018 Labeler - The Procter & Gamble Manufacturing Company (004238200)

