Tolnaftate
- Product NDC
- 55301-132
- Requested package NDC
- 55301-132-46
- 11-digit product format
- 553010132
- Labeler code
- 55301
- Product ID
- 55301-132_c79331e3-6e00-2fa9-e053-2995a90a4094
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Antifungal Powder Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- ARMY & AIR FORCE EXCHANGE SERVICE
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2012-01-03
- Marketing end
- 0000-00-00
- Substance
- TOLNAFTATE
- Active strength
- 1 g/130g
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 55301-132 | 55301-132-46 | D | Discontinued by firm | 2026-10-05 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 55301-132-46 | 55301013246 | 130 g in 1 CAN (55301-132-46) | 130 g | 2012-01-03 | 0000-00-00 | No | No | Current |