NDC 86048-004 - SPOTS and VELVETS Aquarium Cure Program FRESH
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
- 86048-004
- Package NDCs from labels
- 86048-004-01
- Manufacturer
- Prodibio SAS
- Effective date
- 2015-09-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SPOTS and VELVETS Aquarium Cure Program FRESH - Prodibio SAS | Prodibio SAS | 2015-09-03 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86048-004-01 | SPOTS and VELVETS Aquarium Cure Program FRESH | 1 in 1 BOX | KIT | 1 | 2 | |
| 86048-005-01 | SPOTS and VELVETS Aquarium Cure Program FRESH | 0.8 mL in 1 VIAL, SINGLE-USE | SOLUTION | 2.4 mL | 2.5 mg in 1mL | 2 |
| 86048-012-01 | SPOTS and VELVETS Aquarium Cure Program FRESH | 0.6 mL in 1 VIAL, SINGLE-USE | SOLUTION | 1.2 mL | 2.5 mg in 1mL | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 86048-004 | SPOTS AND VELVETS AQUARIUM CURE PROGRAM FRESH (ACRIFLAVINE HYDROCHLORIDE, GENTIAN VIOLET, MALACHITE GREEN OXALATE, METHYLENE BLUE) KIT [PRODIBIO SAS] | 2 | 3 package rows | 20150903_b902af0a-8236-4d43-926a-3f661f1ca5dc.zip |
DailyMed Socrata Ingredients#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| URELLE | HYOSCYAMINE SULFATE, METHENAMINE, METHYLENE BLUE, PHENYL SALICYLATE, AND SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE | Viatris Specialty LLC | 1d80a11c-6f86-403b-85d4-32ec1924dbe9 | 2015-01-13 | Warnings, Adverse reactions | T42P99266K |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.