- 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
CVS/pharmacy Maximum Strength Dandruff shampoo helps reduce itching, flaking, scaling, irritation and redness
due to severe dandruff and seborrheic dermatitis. This advanced formula cleanses and help relieve itch, leaving hair soft and manageable.
Helps control and protect against dandruff from the first wash
Gentle and pH balanced for everyday use, even for permed or color-treated hair*This product is not manufactured or distributed by Procter + Gamble, owner of the registered trademark Head + Shoulders
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
2013CVS/pharmacy
www.cvs.com 1-800-shop-CVS
Made in the U.S.A. of U.S. and imported parts
- principal display panel
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INGREDIENTS AND APPEARANCE
DANDRUFF
selenium sulfide shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-589 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:59779-589-15 420 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 12/09/2012 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 12/09/2012 Labeler - CVS (062312574) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(59779-589) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 088520668 manufacture(59779-589)