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TINEACIDE
TINEACIDE - 63347-502-01 - (MICONAZOLE NITRATE)
Drug Information of TINEACIDE
| Product NDC: | 63347-502 |
| Proprietary Name: | TINEACIDE |
| Non Proprietary Name: | MICONAZOLE NITRATE |
| Active Ingredient(s): | .7 g/35g & nbsp; MICONAZOLE NITRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TINEACIDE
| Product NDC: | 63347-502 |
| Labeler Name: | Blaine Labs Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130601 |
Package Information of TINEACIDE
| Package NDC: | 63347-502-01 |
| Package Description: | 35 g in 1 BOTTLE (63347-502-01) |
NDC Information of TINEACIDE
| NDC Code | 63347-502-01 |
| Proprietary Name | TINEACIDE |
| Package Description | 35 g in 1 BOTTLE (63347-502-01) |
| Product NDC | 63347-502 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MICONAZOLE NITRATE |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130601 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Blaine Labs Inc. |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | .7 |
| Strength Unit | g/35g |
| Pharmaceutical Classes |
