Tolfyra
- Product NDC
- 85477-331
- 11-digit product format
- 854770331
- Labeler code
- 85477
- Product ID
- 85477-331_9a2daff0-df69-4dd4-9b2b-84d1b74de374
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Tolnaftate
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Oncora Pharma, LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-05-01
- Substance
- TOLNAFTATE
- Active strength
- .3 g/30mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Tolfyra
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TOLNAFTATE | .3 g/30mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 06KB629TKV |
| Rxcui | 313423 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 85477-331-01 | Tolfyra | 30 mL in 1 BOTTLE, WITH APPLICATOR | LIQUID | 30 | | 6 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 85477-331-01 | 85477033101 | 30 mL in 1 BOTTLE, WITH APPLICATOR (85477-331-01) | 30 ml | 2026-05-01 | No | No | Current |