- Active Ingredients
- Purpose
- Use
- Warnings
- Stop use and ask a doctor if
- Keep out of reach of children
- Other information
- Directions
- Other information
- inactive ingredient
- SPL UNCLASSIFIED SECTION
- principal display panel
-
INGREDIENTS AND APPEARANCE
ISOPROPYL RUBBING ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37205-012 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37205-012-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/09/2015 2 NDC:37205-012-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 05/09/2015 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 05/09/2012 Labeler - Cardinal Health (097537435) Registrant - Vi-Jon Inc (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, Inc 790752542 manufacture(37205-012)