Tolnafate
- Product NDC
- 79481-0592
- Requested package NDC
- 79481-0592-1
- 11-digit product format
- 794810592
- Labeler code
- 79481
- Product ID
- 79481-0592_dd2fa6a2-2ba6-4333-e053-2a95a90a9790
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate Powder Spray
- Dosage form
- AEROSOL, SPRAY
- Route
- TOPICAL
- Labeler
- Meijer Distribution Inc.
- Application
- part333C
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-03-11
- Marketing end
- 0000-00-00
- Substance
- TOLNAFTATE
- Active strength
- 1 g/130g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 79481-0592 | TOLNAFATE (TOLNAFTATE POWDER SPRAY) AEROSOL, SPRAY [MEIJER DISTRIBUTION INC.] | 5 | Legacy NDC | 20241016_db03a4b1-72b1-2fce-e053-2a95a90a0faf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 79481-0592-1 | 79481059201 | 130 g in 1 CAN (79481-0592-1) | 130 g | 2022-03-11 | 0000-00-00 | No | No | Current |