Okdiary Nail Fungus Treatment
- Product NDC
- 87204-221
- 11-digit product format
- 872040221
- Labeler code
- 87204
- Product ID
- 87204-221_5e04c997-c5a4-7eaf-e063-6294a90afccf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Undecylenic Acid 25%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Guangzhou Huixue Biotechnology Co., Ltd.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-04
- Marketing end
- 2027-10-10
- Substance
- UNDECYLENIC ACID
- Active strength
- .25 mg/30mL
- NDC exclude flag
- No
- 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
- Okdiary Nail Fungus Treatment
Active Ingredients#
| Ingredient | Strength |
|---|---|
| UNDECYLENIC ACID | .25 mg/30mL |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 87204-221-01 | 87204022101 | 30 mL in 1 BOTTLE, PLASTIC (87204-221-01) | 30 ml | 2026-10-04 | 2027-10-10 | No | No | Historical |