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Isopropyl Alcohol - 12745-105-06 - (Isopropyl Alcohol)

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Drug Information of Isopropyl Alcohol

Product NDC: 12745-105
Proprietary Name: Isopropyl Alcohol
Non Proprietary Name: Isopropyl Alcohol
Active Ingredient(s): 70.14    g/100mL & nbsp;   Isopropyl Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Isopropyl Alcohol

Product NDC: 12745-105
Labeler Name: Medical Chemical Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part344
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19540615

Package Information of Isopropyl Alcohol

Package NDC: 12745-105-06
Package Description: 18927 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (12745-105-06)

NDC Information of Isopropyl Alcohol

NDC Code 12745-105-06
Proprietary Name Isopropyl Alcohol
Package Description 18927 mL in 1 CONTAINER, FLEXIBLE INTERMEDIATE BULK (12745-105-06)
Product NDC 12745-105
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Isopropyl Alcohol
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 19540615
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Medical Chemical Corporation
Substance Name ISOPROPYL ALCOHOL
Strength Number 70.14
Strength Unit g/100mL
Pharmaceutical Classes

Complete Information of Isopropyl Alcohol


General Information