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Isopropyl Alcohol - 53329-800-04 - (Isopropyl Alcohol)

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Drug Information of Isopropyl Alcohol

Product NDC: 53329-800
Proprietary Name: Isopropyl Alcohol
Non Proprietary Name: Isopropyl Alcohol
Active Ingredient(s): 70    mL/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: 53329-800
Labeler Name: Medline Industries, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20090216

Package Information of Isopropyl Alcohol

Package NDC: 53329-800-04
Package Description: 118 mL in 1 BOTTLE, SPRAY (53329-800-04)

NDC Information of Isopropyl Alcohol

NDC Code 53329-800-04
Proprietary Name Isopropyl Alcohol
Package Description 118 mL in 1 BOTTLE, SPRAY (53329-800-04)
Product NDC 53329-800
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Isopropyl Alcohol
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20090216
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Medline Industries, Inc.
Substance Name ISOPROPYL ALCOHOL
Strength Number 70
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Isopropyl Alcohol


General Information