NDC 75841-199 - TOLNAFTATE ANTIFUNGAL
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 75841-199
- Manufacturer
- Major Pharmaceuticals | GCP Laboratories
- Effective date
- 2021-12-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| TOLNAFTATE ANTIFUNGAL - Major Pharmaceuticals | GCP Laboratories | Major Pharmaceuticals | GCP Laboratories | 2021-12-21 | HUMAN OTC DRUG LABEL |
| Anti-Fungal - Rugby Laboratories | GCP Laboratories | Rugby Laboratories | GCP Laboratories | 2021-12-21 | HUMAN OTC DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| TOLNAFTATE | ACTIVE INGREDIENT | 06KB629TKV | TOLNAFTATE ANTIFUNGAL (TOLNAFTATE) POWDER [MAJOR PHARMACEUTICALS INC.] | 1 | |
| TOLNAFTATE | ACTIVE INGREDIENT | 06KB629TKV | ANTI-FUNGAL (TOLNAFTATE) POWDER [RUGBY LABORATORIES] | 1 | |
| TOLNAFTATE | ACTIVE MOIETY | 06KB629TKV | TOLNAFTATE ANTIFUNGAL (TOLNAFTATE) POWDER [MAJOR PHARMACEUTICALS INC.] | 1 | |
| TOLNAFTATE | ACTIVE MOIETY | 06KB629TKV | ANTI-FUNGAL (TOLNAFTATE) POWDER [RUGBY LABORATORIES] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | TOLNAFTATE ANTIFUNGAL (TOLNAFTATE) POWDER [MAJOR PHARMACEUTICALS INC.] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | ANTI-FUNGAL (TOLNAFTATE) POWDER [RUGBY LABORATORIES] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | TOLNAFTATE ANTIFUNGAL (TOLNAFTATE) POWDER [MAJOR PHARMACEUTICALS INC.] | 1 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | ANTI-FUNGAL (TOLNAFTATE) POWDER [RUGBY LABORATORIES] | 1 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.