NDC 86077-1040 - HORSEMANS DREAM FUNG-A-WAY
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 86077-1040
- Package NDCs from labels
- 86077-1040-6, 86077-1040-2
- Manufacturer
- Manna Pro Products LLC
- Effective date
- 2025-12-11
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| HORSEMANS DREAM FUNG-A-WAY - Manna Pro Products LLC | Manna Pro Products LLC | 2025-12-11 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86077-1040-2 | HORSEMANS DREAM FUNG-A-WAY | 907.2 mL in 1 BOTTLE | SOLUTION | 907.2 | 21 | |
| 86077-1040-6 | HORSEMANS DREAM FUNG-A-WAY | 453.6 mL in 1 BOTTLE | SOLUTION | 453.6 | 21 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 86077-1040 | HORSEMANS DREAM FUNG-A-WAY (BENZALKONIUM CHLORIDE) SOLUTION [MANNA PRO PRODUCTS LLC] | 20 | 2 package rows | 20241216_7edfd175-6c3d-471c-8d97-6143dfe939fb.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.