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ULTRACEPT
ULTRACEPT - 0064-1090-59 - (ethyl alcohol)
Drug Information of ULTRACEPT
| Product NDC: | 0064-1090 |
| Proprietary Name: | ULTRACEPT |
| Non Proprietary Name: | ethyl alcohol |
| Active Ingredient(s): | .7 g/g & nbsp; ethyl alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ULTRACEPT
| Product NDC: | 0064-1090 |
| Labeler Name: | Healthpoint, Ltd. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20091109 |
Package Information of ULTRACEPT
| Package NDC: | 0064-1090-59 |
| Package Description: | 50 g in 1 BOTTLE (0064-1090-59) |
NDC Information of ULTRACEPT
| NDC Code | 0064-1090-59 |
| Proprietary Name | ULTRACEPT |
| Package Description | 50 g in 1 BOTTLE (0064-1090-59) |
| Product NDC | 0064-1090 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ethyl alcohol |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091109 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Healthpoint, Ltd. |
| Substance Name | ALCOHOL |
| Strength Number | .7 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
