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,
69423-293-12,
69423-293-25, view more69423-293-37, 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
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated March 2, 2023
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- Official Label (Printer Friendly)
- 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 WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) GLYCOL DISTEARATE (UNII: 13W7MDN21W) 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) 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 3 NDC:69423-293-38 380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 4 NDC:69423-293-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 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 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)