NDC | 12745-105-01, 12745-105-02, 12745-105-03, 12745-105-04, 12745-105-05, 12745-105-06, 12745-105-07 |
Set ID | a04239d8-0fa9-4c00-aa81-d7a1242bc931 |
Category | HUMAN OTC DRUG LABEL |
Packager | Medical Chemical Corporation |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART344 |
- PURPOSE
- INDICATIONS & USAGE
- ACTIVE INGREDIENT
- KEEP OUT OF REACH OF CHILDREN
- USER SAFETY WARNINGS
- WARNINGS
- INACTIVE INGREDIENT
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
ISOPROPYL ALCOHOL
isopropyl alcohol liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:12745-105 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL 70.14 g in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:12745-105-01 946 mL in 1 BOTTLE, PLASTIC; Type 1: Convenience Kit of Co-Package 06/15/1954 2 NDC:12745-105-03 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/15/1954 3 NDC:12745-105-04 3785 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/15/1954 4 NDC:12745-105-05 18927 mL in 1 CONTAINER; Type 0: Not a Combination Product 06/15/1954 5 NDC:12745-105-06 18927 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK; Type 0: Not a Combination Product 06/15/1954 6 NDC:12745-105-07 208198 mL in 1 DRUM; Type 0: Not a Combination Product 06/15/1954 7 NDC:12745-105-08 473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/15/1954 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part344 06/15/1954 Labeler - Medical Chemical Corporation (008496861) Establishment Name Address ID/FEI Business Operations Medical Chemical Corporation 008496861 manufacture(12745-105)