Nail Fungus Treatment Solution
- Product NDC
- 88021-001
- 11-digit product format
- 880210001
- Labeler code
- 88021
- Product ID
- 88021-001_5d50f95e-eb6d-835c-e063-6394a90a1034
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Undecylenic Acid
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Nanyang Jingfutang Pharmaceutical Co., Ltd
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-08
- Substance
- UNDECYLENIC ACID; TOLNAFTATE
- Active strength
- 25; 1 g/100mL; g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nail Fungus Treatment Solution
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| UNDECYLENIC ACID | 25 g/100mL |
| TOLNAFTATE | 1 g/100mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 88021-001-01 | 88021000101 | 30 mL in 1 BOTTLE (88021-001-01) | 30 ml | 2026-10-08 | No | No | Current |