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Alcohol Prep - 76161-001-01 - (ISOPROPYL ALCOHOL)

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Drug Information of Alcohol Prep

Product NDC: 76161-001
Proprietary Name: Alcohol Prep
Non Proprietary Name: ISOPROPYL ALCOHOL
Active Ingredient(s): .7    mL/1 & nbsp;   ISOPROPYL ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): SWAB
Coding System: National Drug Codes(NDC)

Labeler Information of Alcohol Prep

Product NDC: 76161-001
Labeler Name: KYJ Medical Products Co.,Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: part344
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110420

Package Information of Alcohol Prep

Package NDC: 76161-001-01
Package Description: 1 SWAB in 1 PACKAGE (76161-001-01)

NDC Information of Alcohol Prep

NDC Code 76161-001-01
Proprietary Name Alcohol Prep
Package Description 1 SWAB in 1 PACKAGE (76161-001-01)
Product NDC 76161-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ISOPROPYL ALCOHOL
Dosage Form Name SWAB
Route Name TOPICAL
Start Marketing Date 20110420
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name KYJ Medical Products Co.,Ltd.
Substance Name ISOPROPYL ALCOHOL
Strength Number .7
Strength Unit mL/1
Pharmaceutical Classes

Complete Information of Alcohol Prep


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