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ETHYL ALCOHOL
ETHYL ALCOHOL - 21749-525-89 - (ALCOHOL)
Drug Information of ETHYL ALCOHOL
| Product NDC: | 21749-525 |
| Proprietary Name: | ETHYL ALCOHOL |
| Non Proprietary Name: | ALCOHOL |
| Active Ingredient(s): | .7 mL/mL & nbsp; ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ETHYL ALCOHOL
| Product NDC: | 21749-525 |
| Labeler Name: | GOJO Industries, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20100526 |
Package Information of ETHYL ALCOHOL
| Package NDC: | 21749-525-89 |
| Package Description: | 1250 mL in 1 BOTTLE (21749-525-89) |
NDC Information of ETHYL ALCOHOL
| NDC Code | 21749-525-89 |
| Proprietary Name | ETHYL ALCOHOL |
| Package Description | 1250 mL in 1 BOTTLE (21749-525-89) |
| Product NDC | 21749-525 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ALCOHOL |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20100526 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | GOJO Industries, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | mL/mL |
| Pharmaceutical Classes |
