PureWellness FUNGAL FUSION Antifungal and Antimicrobial Kit
- Product NDC
- 87817-200
- 11-digit product format
- 878170200
- Labeler code
- 87817
- Product ID
- 87817-200_624ed566-a989-47ee-b2c0-f4fcb37ed4d4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- FUNGAL FUSION Antifungal and Antimicrobial Kit
- Dosage form
- KIT
- Labeler
- PureWellness LLC
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-07-06
- 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
- PureWellness FUNGAL FUSION Antifungal and Antimicrobial Kit
- Listing expiration
- 2027-12-31
Harmonized RxCUI identifiers#
Harmonized SPL set identifiers#
| Identifier | FDA.report destination |
|---|---|
| 25db8c55-0fa9-4795-8e05-4d3a7aaf0148 | Available on FDA.report |
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 | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 87817-200-01 | 87817020001 | 1 KIT in 1 CARTON (87817-200-01) * 1 BOTTLE in 1 KIT (87817-110-01) / 57 g in 1 BOTTLE * 1 BOTTLE, GLASS in 1 KIT (87817-101-01) / 30 mL in 1 BOTTLE, GLASS | 1 kit | 2026-07-06 | No | No | Current |