Label: HEAD AND SHOULDERS 2IN1 MEN ADVANCED SERIES PURE SPORT OLD SPICE- pyrithione zinc lotion/shampoo
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NDC Code(s):
69423-293-01,
69423-293-02,
69423-293-11,
69423-293-12, view more69423-293-25, 69423-293-37, 69423-293-38, 69423-293-61, 69423-293-65, 69423-293-83, 69423-293-90, 69423-293-93
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated August 29, 2024
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
- Directions
- Inactive ingredients
- Questions (or comments)?
- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 370 mL Bottle Label
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS 2IN1 MEN ADVANCED SERIES PURE SPORT OLD SPICE
pyrithione zinc lotion/shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-293 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 GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) 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) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-293-93 930 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/29/2018 2 NDC:69423-293-25 250 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 12/01/2024 3 NDC:69423-293-38 380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 12/01/2024 4 NDC:69423-293-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 01/01/2025 5 NDC:69423-293-90 90 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 10/01/2022 6 NDC:69423-293-12 1280 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/29/2018 7 NDC:69423-293-01 2 in 1 CELLO PACK 01/15/2020 7 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 8 NDC:69423-293-02 2 in 1 CELLO PACK 01/15/2020 8 930 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 9 NDC:69423-293-61 613 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2022 10 NDC:69423-293-83 835 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/29/2022 11 NDC:69423-293-37 370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2022 12 NDC:69423-293-11 1180 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 06/01/2023 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)