Label: HEAD AND SHOULDERS DEEP MOISTURE 2IN1- pyrithione zinc lotion/shampoo
- NDC Code(s): 69423-248-38, 69423-248-65
- 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 31, 2023
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Inactive ingredients
Water, sodium laureth sulfate, cocamide MEA, sodium xylenesulfonate, zinc carbonate, glycol distearate, sodium lauryl sulfate, dimethicone, cocamidopropyl betaine, sodium chloride, fragrance, guar hydroxypropyltrimonium chloride, sodium benzoate, polyquaternium-10, stearyl alcohol, magnesium carbonate hydroxide, cetyl alcohol, persea gratissima (avocado) oil, methylchloroisothiazolinone, methylisothiazolinone.
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- PRINCIPAL DISPLAY PANEL - 380 mL Bottle Label
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS DEEP MOISTURE 2IN1
pyrithione zinc lotion/shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-248 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 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) COCO MONOETHANOLAMIDE (UNII: C80684146D) POLYQUATERNIUM-10 (30000 MPA.S AT 2%) (UNII: C7RDC8Y4JS) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) AVOCADO OIL (UNII: 6VNO72PFC1) CETYL ALCOHOL (UNII: 936JST6JCN) 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-248-38 380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/2017 12/01/2024 2 NDC:69423-248-65 650 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/01/2017 08/17/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final M032 12/01/2017 12/01/2024 Labeler - The Procter & Gamble Manufacturing Company (004238200)