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HUSKY 515
HUSKY 515 - 63779-515-62 - (ethanol)
Drug Information of HUSKY 515
| Product NDC: | 63779-515 |
| Proprietary Name: | HUSKY 515 |
| Non Proprietary Name: | ethanol |
| Active Ingredient(s): | 600 mL/L & nbsp; ethanol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of HUSKY 515
| Product NDC: | 63779-515 |
| Labeler Name: | Canberra Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19981028 |
Package Information of HUSKY 515
| Package NDC: | 63779-515-62 |
| Package Description: | .237 L in 1 BOTTLE (63779-515-62) |
NDC Information of HUSKY 515
| NDC Code | 63779-515-62 |
| Proprietary Name | HUSKY 515 |
| Package Description | .237 L in 1 BOTTLE (63779-515-62) |
| Product NDC | 63779-515 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ethanol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19981028 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Canberra Corporation |
| Substance Name | ALCOHOL |
| Strength Number | 600 |
| Strength Unit | mL/L |
| Pharmaceutical Classes |
