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GOODSENSE Alcohol - 75981-001-00 - (ISOPROPYL ALCOHOL)

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Drug Information of GOODSENSE Alcohol

Product NDC: 75981-001
Proprietary Name: GOODSENSE Alcohol
Non Proprietary Name: ISOPROPYL ALCOHOL
Active Ingredient(s): 70    g/100g & nbsp;   ISOPROPYL ALCOHOL
Administration Route(s): TOPICAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of GOODSENSE Alcohol

Product NDC: 75981-001
Labeler Name: GEISS, DESTIN AND DUNN, INC.
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110630

Package Information of GOODSENSE Alcohol

Package NDC: 75981-001-00
Package Description: 100 PACKET in 1 BOX (75981-001-00) > .5 g in 1 PACKET

NDC Information of GOODSENSE Alcohol

NDC Code 75981-001-00
Proprietary Name GOODSENSE Alcohol
Package Description 100 PACKET in 1 BOX (75981-001-00) > .5 g in 1 PACKET
Product NDC 75981-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ISOPROPYL ALCOHOL
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20110630
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GEISS, DESTIN AND DUNN, INC.
Substance Name ISOPROPYL ALCOHOL
Strength Number 70
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of GOODSENSE Alcohol


General Information