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Up and Up alcohol - 11673-809-30 - (Isopropyl Alcohol)

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Drug Information of Up and Up alcohol

Product NDC: 11673-809
Proprietary Name: Up and Up alcohol
Non Proprietary Name: Isopropyl Alcohol
Active Ingredient(s): 70    mL/100mL & nbsp;   Isopropyl Alcohol
Administration Route(s): TOPICAL
Dosage Form(s): SWAB
Coding System: National Drug Codes(NDC)

Labeler Information of Up and Up alcohol

Product NDC: 11673-809
Labeler Name: Target Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20100101

Package Information of Up and Up alcohol

Package NDC: 11673-809-30
Package Description: 100 PACKET in 1 BOX (11673-809-30) > 1 APPLICATOR in 1 PACKET (11673-809-09) > 5 mL in 1 APPLICATOR

NDC Information of Up and Up alcohol

NDC Code 11673-809-30
Proprietary Name Up and Up alcohol
Package Description 100 PACKET in 1 BOX (11673-809-30) > 1 APPLICATOR in 1 PACKET (11673-809-09) > 5 mL in 1 APPLICATOR
Product NDC 11673-809
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Isopropyl Alcohol
Dosage Form Name SWAB
Route Name TOPICAL
Start Marketing Date 20100101
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Target Corporation
Substance Name ISOPROPYL ALCOHOL
Strength Number 70
Strength Unit mL/100mL
Pharmaceutical Classes

Complete Information of Up and Up alcohol


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