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TRISEPTIN
TRISEPTIN - 0064-1040-32 - (ETHYL ALCOHOL)
Drug Information of TRISEPTIN
| Product NDC: | 0064-1040 |
| Proprietary Name: | TRISEPTIN |
| Non Proprietary Name: | ETHYL ALCOHOL |
| Active Ingredient(s): | .61 g/g & nbsp; ETHYL ALCOHOL |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TRISEPTIN
| Product NDC: | 0064-1040 |
| Labeler Name: | HEALTHPOINT, LTD |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333E |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20040301 |
Package Information of TRISEPTIN
| Package NDC: | 0064-1040-32 |
| Package Description: | 837 g in 1 BOTTLE, PLASTIC (0064-1040-32) |
NDC Information of TRISEPTIN
| NDC Code | 0064-1040-32 |
| Proprietary Name | TRISEPTIN |
| Package Description | 837 g in 1 BOTTLE, PLASTIC (0064-1040-32) |
| Product NDC | 0064-1040 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ETHYL ALCOHOL |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20040301 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | HEALTHPOINT, LTD |
| Substance Name | ALCOHOL |
| Strength Number | .61 |
| Strength Unit | g/g |
| Pharmaceutical Classes |
