Label: HEAD AND SHOULDERS 2IN1 MEN ADVANCED SERIES FULL AND THICK- pyrithione zinc lotion/shampoo
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NDC Code(s):
69423-329-37,
69423-329-38,
69423-329-61,
69423-329-65, view more69423-329-83, 69423-329-93
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
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 28, 2023
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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, sodium laureth sulfate, glycol distearate, sodium chloride, zinc carbonate, dimethicone, cocamidopropyl betaine, sodium xylenesulfonate, fragrance, sodium benzoate, menthol, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, caffeine, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33
- 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 FULL AND THICK
pyrithione zinc lotion/shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-329 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 SODIUM LAURYL SULFATE (UNII: 368GB5141J) WATER (UNII: 059QF0KO0R) SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0) GLYCOL DISTEARATE (UNII: 13W7MDN21W) ZINC CARBONATE (UNII: EQR32Y7H0M) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM BENZOATE (UNII: OJ245FE5EU) MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C RED NO. 33 (UNII: 9DBA0SBB0L) MENTHOL (UNII: L7T10EIP3A) GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A) CAFFEINE (UNII: 3G6A5W338E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-329-38 380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 12/01/2024 2 NDC:69423-329-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/29/2018 12/01/2024 3 NDC:69423-329-93 930 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 11/29/2018 4 NDC:69423-329-37 370 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2023 5 NDC:69423-329-61 613 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 02/01/2023 6 NDC:69423-329-83 835 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 02/01/2023 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)