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Ben E.Keith
Ben E.Keith - 50980-056-19 - (Ethyl Alcohol)
Drug Information of Ben E.Keith
| Product NDC: | 50980-056 |
| Proprietary Name: | Ben E.Keith |
| Non Proprietary Name: | Ethyl Alcohol |
| Active Ingredient(s): | 62 mL/100mL & nbsp; Ethyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ben E.Keith
| Product NDC: | 50980-056 |
| Labeler Name: | Ben E. Keith |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090102 |
Package Information of Ben E.Keith
| Package NDC: | 50980-056-19 |
| Package Description: | 237 mL in 1 BOTTLE, PUMP (50980-056-19) |
NDC Information of Ben E.Keith
| NDC Code | 50980-056-19 |
| Proprietary Name | Ben E.Keith |
| Package Description | 237 mL in 1 BOTTLE, PUMP (50980-056-19) |
| Product NDC | 50980-056 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethyl Alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20090102 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Ben E. Keith |
| Substance Name | ETHANOL |
| Strength Number | 62 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |
