- claims
- Active ingredient
- Purpose
- Use
- Warnings
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children
- Directions
- Inactive ingredients
- questions or comments?
- Warnings and claims
- Dislcaimer
- ADVERSE REACTIONS
- principal display panel
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INGREDIENTS AND APPEARANCE
ULTRA
chloroxylenol 0.3% liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:30142-562 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CHLOROXYLENOL (UNII: 0F32U78V2Q) (CHLOROXYLENOL - UNII:0F32U78V2Q) CHLOROXYLENOL 3.09 g in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U) LAURAMINE OXIDE (UNII: 4F6FC4MI8W) SODIUM LAURETH SULFATE (UNII: BPV390UAP0) SODIUM LAURYL SULFATE (UNII: 368GB5141J) ALCOHOL (UNII: 3K9958V90M) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM CHLORIDE (UNII: 451W47IQ8X) SODIUM XYLENESULFONATE (UNII: G4LZF950UR) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) FD&C YELLOW NO. 5 (UNII: I753WB2F1M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:30142-562-50 709 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product 04/29/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/29/2015 Labeler - Kroger Co (006999528) Registrant - Vi-Jon (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon 088520668 manufacture(30142-562)