- Active Ingredients
- Purpose
- Uses
- Warnings
- ask a doctor before use
- when using this product
- stop use and ask a doctor if
- Keep out of reach of children
- Other information
- Directions
- Other information
- Inactive ingredients
- Adverse Reactions
- principal display panel
- principal display panel
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INGREDIENTS AND APPEARANCE
ISOPROPYL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0869-0211 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 924 mg in 1 mL Inactive Ingredients Ingredient Name Strength FD&C BLUE NO. 1 (UNII: H3R47K3TBD) METHYL SALICYLATE (UNII: LAV5U5022Y) WATER (UNII: 059QF0KO0R) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0869-0211-43 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/30/2004 2 NDC:0869-0211-40 355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/30/2004 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 09/30/2004 Labeler - Vi-Jon, LLC (790752542) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(0869-0211)