Label: DANDRUFF- selenium sulfide shampoo
- NDC Code(s): 30142-816-15
- Packager: Kroger
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated September 11, 2024
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- Active ingredient
- Purpose
- Use
- Warnings
- Ask a doctor before use if
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
- Directions
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Inactive ingredients
water, ammonium laureth sulfate, ammonium lauryl sulfate, glycol distearate, cocamide MEA, ammonium xylenesulfonate, sodium citrate, fragrance, amodimethicone, cetyl alcohol, sodium chloride, citric acid, sodium benzoate, stearyl alcohol, disodium EDTA, hydrogen peroxide, hydroxypropyl methylcellulose, methylchlorisothiazolinone, methylisothiazolinone, red 4
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SPL UNCLASSIFIED SECTION
advanced solution
dandruff shampoo
Dermatologist Tested
Maximum Strength*Head + Shoulder is a registered trademark of Procter + Gamble, Cincinnati, OH 45202. Procter + Gamble is not affiliated with The Kroger Co., or this product.
DISTRIBUTED BY THE KROGER Co.,
CINCINNATI, OHIO 45202
Quality Guarantee
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INGREDIENTS AND APPEARANCE
DANDRUFF
selenium sulfide shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-816 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q) SELENIUM SULFIDE 10 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) AMMONIUM LAURETH-3 SULFATE (UNII: 896SJ235FN) AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B) GLYCOL DISTEARATE (UNII: 13W7MDN21W) COCO MONOETHANOLAMIDE (UNII: C80684146D) AMMONIUM XYLENESULFONATE (UNII: 4FZY6L6XCM) SODIUM CITRATE (UNII: 1Q73Q2JULR) AMODIMETHICONE (800 CST) (UNII: 363Z2T48P7) CETYL ALCOHOL (UNII: 936JST6JCN) SODIUM CHLORIDE (UNII: 451W47IQ8X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) SODIUM BENZOATE (UNII: OJ245FE5EU) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) EDETATE DISODIUM (UNII: 7FLD91C86K) HYDROGEN PEROXIDE (UNII: BBX060AN9V) HYPROMELLOSES (UNII: 3NXW29V3WO) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C RED NO. 4 (UNII: X3W0AM1JLX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-816-15 420 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2013 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M032 06/01/2013 Labeler - Kroger (006999528) Registrant - Consumer Product Partners, LLC (119091520) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091520 manufacture(30142-816) Establishment Name Address ID/FEI Business Operations Consumer Product Partners, LLC 119091514 manufacture(30142-816) Establishment Name Address ID/FEI Business Operations RWM TECHNOLOGIES LLC 626626969 manufacture(30142-816)