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ethyl alcohol
ethyl alcohol - 50730-8672-0 - (ethyl alcohol)
Drug Information of ethyl alcohol
| Product NDC: | 50730-8672 |
| Proprietary Name: | ethyl alcohol |
| Non Proprietary Name: | ethyl alcohol |
| Active Ingredient(s): | .7 g/g & nbsp; ethyl alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ethyl alcohol
| Product NDC: | 50730-8672 |
| Labeler Name: | H and P Industries, Inc. dba Triad Group |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 19971117 |
Package Information of ethyl alcohol
| Package NDC: | 50730-8672-0 |
| Package Description: | 72 PACKET in 1 BOX (50730-8672-0) > 5 g in 1 PACKET |
NDC Information of ethyl alcohol
| NDC Code | 50730-8672-0 |
| Proprietary Name | ethyl alcohol |
| Package Description | 72 PACKET in 1 BOX (50730-8672-0) > 5 g in 1 PACKET |
| Product NDC | 50730-8672 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ethyl alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 19971117 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | H and P Industries, Inc. dba Triad Group |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
