NDC 17030-081 - Renal K Plus
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
- 17030-081
- Package NDCs from labels
- 17030-081-05
- Manufacturer
- Vetoquinol USA, Inc. | Vetoquinol N.-A. INC
- Effective date
- 2020-02-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Renal K Plus - Vetoquinol USA, Inc. | Vetoquinol N.-A. INC | Vetoquinol USA, Inc. | Vetoquinol N.-A. INC | 2020-02-13 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 17030-081-05 | Renal K Plus | 142 g in 1 TUBE | GEL | 142 | 1 |
DailyMed Dashboard NDC Coverage#
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.
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|---|---|---|---|---|---|---|
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| Dr.Jucre Rebirth | NIACINAMIDE, ADENOSINE | NATURECELL CO., LTD. | 2ab449f5-02eb-b075-e063-6394a90a9b50 | 2025-01-02 | Warnings | 25X51I8RD4 |
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| TheraTears Extra | CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED | MEDTECH PRODUCTS INC | f1845041-9d8d-42a0-a2cb-68def7a5aac7 | 2024-12-13 | Warnings | K679OBS311 |
| Cyanocobalamin | CYANOCOBALAMIN | Fresenius Kabi USA, LLC | 8b1cdee5-3368-40e4-90bf-31a64df1f38a | 2024-12-12 | Warnings, Adverse reactions | P6YC3EG204 |
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| Ventrixyl | FOLIC ACID | PureTek Corporation | c29dc729-93be-2a20-e053-2a95a90a8ca3 | 2024-12-03 | Warnings, Adverse reactions | 25X51I8RD4 935E97BOY8 P6YC3EG204 68Y4CF58BV |
| FOLIC ACID | FOLIC ACID | SUNRISE PHARMACEUTICAL, INC. | 6854412b-7ecb-4107-85eb-730f14e23f06 | 2024-12-03 | Warnings, Adverse reactions | 935E97BOY8 |
| Folitin-Z | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | bb141ac2-e5df-4df4-e053-2995a90a6e72 | 2024-12-02 | Warnings, Adverse reactions | 25X51I8RD4 935E97BOY8 6SO6U10H04 P6YC3EG204 68Y4CF58BV |
| Davimet with Iron | IRON, FOLATE | PureTek Corporation | 1445921b-5bf4-ea48-e063-6294a90abb1a | 2024-11-27 | Warnings, Adverse reactions | 25X51I8RD4 68Y4CF58BV |
| Foliflex | FERROUS FUMARATE, FOLIC ACID | PureTek Corporation | cba98d1a-8cf9-39d9-e053-2995a90ae8bb | 2024-11-27 | Warnings, Adverse reactions | 25X51I8RD4 935E97BOY8 6SO6U10H04 P6YC3EG204 68Y4CF58BV |
| PhysiciansCare Ophthalmic Solution Eyewash Purified Water, 98.3% | PURIFIED WATER 98.3% | Acme United Corporation | 9248ee71-2d47-620d-e053-2995a90af5c8 | 2024-11-26 | Warnings | 059QF0KO0R |
| PhysiciansCare Ophthalmic Solution Eyewash | PURIFIED WATER 98.3% | Acme United Corporation | cca454e0-b2bd-4215-bc06-426fcc3f7bd6 | 2024-11-26 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.