Label: HEAD AND SHOULDERS CHARCOAL DAILY- pyrithione zinc lotion/shampoo
- NDC Code(s): 69423-278-37, 69423-278-38, 69423-278-65
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated May 22, 2024
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- Active ingredient
- Purpose
- Uses
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Inactive ingredients
Water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, sodium chloride, zinc carbonate, cocamidopropyl betaine, sodium xylenesulfonate, fragrance, dimethicone, menthol, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide,methylchloroisothiazolinone, methylisothiazolinone, charcoal extract, yellow5, red 33, blue 1
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- PRINCIPAL DISPLAY PANEL - 370 mL Bottle Label
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS CHARCOAL DAILY
pyrithione zinc lotion/shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-278 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 MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) SODIUM LAURYL SULFATE (UNII: 368GB5141J) ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) GLYCOL DISTEARATE (UNII: 13W7MDN21W) D&C RED NO. 33 (UNII: 9DBA0SBB0L) ZINC CARBONATE (UNII: EQR32Y7H0M) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) DIMETHICONE (UNII: 92RU3N3Y1O) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) SODIUM BENZOATE (UNII: OJ245FE5EU) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-278-38 380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/15/2018 12/02/2024 2 NDC:69423-278-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/15/2018 12/07/2020 3 NDC:69423-278-37 370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/15/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 11/15/2018 Labeler - The Procter & Gamble Manufacturing Company (004238200)