NDC | 33992-0864-1, 33992-0864-3, 33992-0864-4 |
Set ID | 489a1918-e008-42ea-a559-82d558095f00 |
Category | HUMAN OTC DRUG LABEL |
Packager | Greenbrier International, Inc. |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART333A |
- Active ingredient
- 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.
- Caution
- Directions
- Other Information
- Inactive ingredient
- adverse reaction
- principal display panel
-
INGREDIENTS AND APPEARANCE
50% RUBBING
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:33992-0864 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:33992-0864-3 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/08/2014 2 NDC:33992-0864-1 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/08/2014 3 NDC:33992-0864-4 710 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/08/2014 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 10/08/2014 Labeler - Greenbrier International, Inc. (610322518) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LLC 790752542 manufacture(33992-0864)