Label: HEAD AND SHOULDERS CLINICAL STRENGTH DANDRUFF DEFENSE ADVANCED OIL CONTROL- selenium sulfide lotion/shampoo
- NDC Code(s): 69423-525-01, 69423-525-40
- Packager: The Procter & Gamble Manufacturing Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 4, 2024
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- SPL UNCLASSIFIED SECTION
- Active ingredient
- Purpose
- Uses
- Warnings
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Inactive ingredients
Water, ammonium laureth sulfate, ammonium lauryl sulfate, glycol distearate, cocamide MEA, ammonium xylenesulfonate, fragrance, sodium citrate, dimethicone, cetyl alcohol, citric acid, sodium chloride, sodium benzoate, disodium EDTA, stearyl alcohol, hydroxypropyl methylcellulose, methylchloroisothiazolinone, methylisothiazolinone, red 4.
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - BOTTLE LABEL
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INGREDIENTS AND APPEARANCE
HEAD AND SHOULDERS CLINICAL STRENGTH DANDRUFF DEFENSE ADVANCED OIL CONTROL
selenium sulfide lotion/shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69423-525 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 EDETATE DISODIUM (UNII: 7FLD91C86K) COCO MONOETHANOLAMIDE (UNII: C80684146D) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) CETYL ALCOHOL (UNII: 936JST6JCN) WATER (UNII: 059QF0KO0R) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) GLYCOL DISTEARATE (UNII: 13W7MDN21W) SODIUM CHLORIDE (UNII: 451W47IQ8X) AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM) DIMETHICONE (UNII: 92RU3N3Y1O) SODIUM BENZOATE (UNII: OJ245FE5EU) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 4 (UNII: X3W0AM1JLX) SODIUM CITRATE (UNII: 1Q73Q2JULR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69423-525-40 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 11/17/2020 2 NDC:69423-525-01 2 in 1 CELLO PACK 01/01/2023 2 400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 11/17/2020 Labeler - The Procter & Gamble Manufacturing Company (004238200)