- 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
-
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
- adverse reaction
- principal display panel
-
INGREDIENTS AND APPEARANCE
DANDRUFF
selenium sulfide shampooProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0869-0816 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:0869-0816-21 88 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/25/2016 2 NDC:0869-0816-15 420 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/25/2016 3 NDC:0869-0816-35 701 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/25/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part358H 09/25/2016 Labeler - Vi-Jon, LLC (790752542) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(0869-0816)