FungiFlush
- Product NDC
- 83311-100
- 11-digit product format
- 833110100
- Labeler code
- 83311
- Product ID
- 83311-100_5def3d42-7a66-e987-e063-6394a90a6471
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Undecylenic acid 25%
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Simple Promise Pte Ltd
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-10-19
- Substance
- UNDECYLENIC ACID
- Active strength
- 25 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
- FungiFlush
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| UNDECYLENIC ACID | 25 g/100mL |
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 | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|
| 83311-100-15 | 83311010015 | 1 BOTTLE, DROPPER in 1 BOX (83311-100-15) / 15 mL in 1 BOTTLE, DROPPER | 2026-10-19 | No | No | Current |