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TINEACIDE
TINEACIDE - 63347-511-03 - (TOLNAFTATE)
Drug Information of TINEACIDE
| Product NDC: | 63347-511 |
| Proprietary Name: | TINEACIDE |
| Non Proprietary Name: | TOLNAFTATE |
| Active Ingredient(s): | 140 mg/15mL & nbsp; TOLNAFTATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of TINEACIDE
| Product NDC: | 63347-511 |
| Labeler Name: | Blaine Labs Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120919 |
Package Information of TINEACIDE
| Package NDC: | 63347-511-03 |
| Package Description: | 15 mL in 1 BOTTLE (63347-511-03) |
NDC Information of TINEACIDE
| NDC Code | 63347-511-03 |
| Proprietary Name | TINEACIDE |
| Package Description | 15 mL in 1 BOTTLE (63347-511-03) |
| Product NDC | 63347-511 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | TOLNAFTATE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20120919 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Blaine Labs Inc. |
| Substance Name | TOLNAFTATE |
| Strength Number | 140 |
| Strength Unit | mg/15mL |
| Pharmaceutical Classes |
