- Active ingredient
- purpose
- Use
- Warnings
- Flammable
- Ask a Doctor before use
- When using theis product
- Stop use and ask a doctor
- Keep out of reach of children
- Caution
- Directions
- Other information
- Inactive ingredients
- SPL UNCLASSIFIED SECTION
- principal display panel
-
INGREDIENTS AND APPEARANCE
70%
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50804-810 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 500 mg in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50804-810-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/08/2010 2 NDC:50804-810-45 946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/08/2010 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 04/08/2010 Labeler - Geiss, Destin & Dunn, Inc (076059836) Registrant - Vi-Jon (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon 790752542 manufacture(50804-810)