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