Label: HEAD AND SHOULDERS 2IN1 CLINICAL STRENGTH DANDRUFF DEFENSE INTENSIVE ITCH RELIEF- selenium sulfide lotion/shampoo
- NDC Code(s): 69423-527-40
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 31, 2025
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
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Inactive ingredients
Water, sodium lauryl sulfate, glycol distearate, sodium chloride, cocamidopropyl betaine, sodium citrate, dimethicone, sodium xylenesulfonate,menthol, fragrance, citric acid, sodium benzoate, tetrasodium EDTA, hydroxypropyl methylcellulose, mentha piperita (peppermint) oil,mentha arvensis leaf oil, red 4.
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 400 mL BOTTLE LABEL
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS 2IN1 CLINICAL STRENGTH DANDRUFF DEFENSE INTENSIVE ITCH RELIEF
selenium sulfide lotion/shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-527 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q) SELENIUM SULFIDE 1 g in 100 mL Inactive Ingredients Ingredient Name Strength MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N) PEPPERMINT OIL (UNII: AV092KU4JH) EDETATE DISODIUM (UNII: 7FLD91C86K) MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) WATER (UNII: 059QF0KO0R) SODIUM LAURYL SULFATE (UNII: 368GB5141J) GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM BENZOATE (UNII: OJ245FE5EU) FD&C RED NO. 4 (UNII: X3W0AM1JLX) SODIUM CITRATE (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-527-40 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/17/2020 12/01/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 11/17/2020 12/01/2026 Labeler - The Procter & Gamble Manufacturing Company (004238200)

