Tinactin
- Product NDC
- 69213-0934
- Requested package NDC
- 69213-0934-2
- 11-digit product format
- 692130934
- Labeler code
- 69213
- Product ID
- 69213-0934_abab2e6e-5832-5362-e053-2995a90a95c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Delpharm Montreal Inc.
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1993-09-23
- Marketing end
- 0000-00-00
- Substance
- TOLNAFTATE
- Active strength
- 10 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 69213-0934-2 | 69213093402 | 1 TUBE in 1 CARTON (69213-0934-2) > 15 g in 1 TUBE | 1 tube | 1993-09-23 | 0000-00-00 | No | No | Current |