- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
- Warnings
- Ask a doctor before use if you have
- Stop use and ask a doctor if:
- When using this product:
- Keep out of the reach of children.
- Directions
- Inactive Ingredient:
- Other Information:
- Label
-
INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:24385-207 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 AMMONIA (UNII: 5138Q19F1X) IODINE (UNII: 9679TC07X4) POTASSIUM IODIDE (UNII: 1C4QK22F9J) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:24385-207-46 59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/30/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part333A 03/25/1998 Labeler - Amerisource Bergen (007914906) Registrant - Humco Holding Group, Inc. (825672884) Establishment Name Address ID/FEI Business Operations Humco Holding Group, Inc. 825672884 manufacture(24385-207) , analysis(24385-207) , pack(24385-207) , label(24385-207)