- ACTIVE INGREDIENT
- INACTIVE INGREDIENT
- PURPOSE
-
WARNINGS
Do not use
- if you are allergic to any of the ingredients
- in the eyes
- over large areas of the body
Ask a doctor before use if you have
- deep or puncture wounds
- animal bites
- serious burns
Stop use and ask a doctor if
- you need to use longer than 1 week
- condition persists or gets worse
- rash or other allergic reaction develops
- KEEP OUT OF REACH OF CHILDREN
- INDICATIONS & USAGE
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
RURINA
sulfate, potassium ion, chloride ion liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71867-0001 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFATE ION (UNII: 7IS9N8KPMG) (SULFATE ION - UNII:7IS9N8KPMG) SULFATE ION 3.6 g in 1 L POTASSIUM CATION (UNII: 295O53K152) (POTASSIUM CATION - UNII:295O53K152) POTASSIUM CATION 0.25 g in 1 L CHLORIDE ION (UNII: Q32ZN48698) (CHLORIDE ION - UNII:Q32ZN48698) CHLORIDE ION 0.11 g in 1 L Inactive Ingredients Ingredient Name Strength MAGNESIUM (UNII: I38ZP9992A) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71867-0001-1 1 L in 1 BOTTLE, GLASS; Type 0: Not a Combination Product 07/01/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 07/01/2017 Labeler - TELOM-X GENE Co., Ltd. (694948208) Registrant - TELOM-X GENE Co., Ltd. (694948208) Establishment Name Address ID/FEI Business Operations TELOM-X GENE Co., Ltd. 694948208 manufacture(71867-0001)