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ZYTEC
ZYTEC - 50021-080-08 - (ETHANOL)
Drug Information of ZYTEC
| Product NDC: | 50021-080 |
| Proprietary Name: | ZYTEC |
| Non Proprietary Name: | ETHANOL |
| Active Ingredient(s): | 224 g/400g & nbsp; ETHANOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | AEROSOL, SPRAY |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZYTEC
| Product NDC: | 50021-080 |
| Labeler Name: | Empack |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part356 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110131 |
Package Information of ZYTEC
| Package NDC: | 50021-080-08 |
| Package Description: | 35 g in 1 CAN (50021-080-08) |
NDC Information of ZYTEC
| NDC Code | 50021-080-08 |
| Proprietary Name | ZYTEC |
| Package Description | 35 g in 1 CAN (50021-080-08) |
| Product NDC | 50021-080 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ETHANOL |
| Dosage Form Name | AEROSOL, SPRAY |
| Route Name | TOPICAL |
| Start Marketing Date | 20110131 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Empack |
| Substance Name | ETHANOL |
| Strength Number | 224 |
| Strength Unit | g/400g |
| Pharmaceutical Classes |
