NDC 59051-9075 - RenaKare
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
- 59051-9075
- Package NDCs from labels
- 59051-9075-1
- Manufacturer
- Neogen Corporation-Mercer Rd | Jungbunzlauer Ladenburg GmbH
- Effective date
- 2023-02-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| RenaKare - Neogen Corporation-Mercer Rd | Jungbunzlauer Ladenburg GmbH | Neogen Corporation-Mercer Rd | Jungbunzlauer Ladenburg GmbH | 2023-02-21 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59051-9075-1 | RenaKare | 113 g in 1 BOTTLE, PLASTIC | POWDER | 113 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 59051-9075 | RENAKARE (POTASSIUM GLUCONATE) POWDER [NEOGEN CORPORATION-MERCER RD] | 3 | 1 package rows | 20230222_af6cbe7b-bdb7-49c5-9ec1-ac3942889366.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| POTASSIUM GLUCONATE | ACTIVE INGREDIENT | 12H3K5QKN9 | RENAKARE (POTASSIUM GLUCONATE) POWDER [NEOGEN CORPORATION-MERCER RD] | 1 | |
| POTASSIUM CATION | ACTIVE MOIETY | 295O53K152 | RENAKARE (POTASSIUM GLUCONATE) POWDER [NEOGEN CORPORATION-MERCER RD] | 1 |
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 |
|---|---|---|---|---|---|---|
| HGH-Pro T020 | HUMAN GROWTH HORMONE, HYPOPHYSIS SUIS, HEPAR SUIS | Guangzhou Renuma Medical Systems Co., Ltd | ec7e7b1b-9b57-4fa2-8017-23e9ec2d1478 | 2017-10-31 | Warnings | 6EC706HI7F |
| Industrotox | GLYCYRRHIZA GLABRA, PLANTAGO MAJOR, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, ARNICA MONTANA, ASCLEPIAS TUBEROSA, BERBERIS VULGARIS, CALENDULA OFFICINALIS, CHAMOMILLA, CHELIDONIUM MAJUS, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, LAPPA MAJOR, NASTURTIUM AQUATICUM, PHYTOLACCA DECANDRA, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, TARAXACUM OFFICINALE, TRIGONELLA FOENUM-GRAECUM, URTICA DIOICA, XANTHOXYLUM FRAXINEUM, SYMPHYTUM OFFICINALE, HEPAR SUIS, LUNG (SUIS), LYMPH NODE (SUIS) | BioActive Nutritional, Inc. | 0722085a-1478-4667-b0c6-3315cff25b08 | 2017-06-16 | Warnings | 6EC706HI7F |
| HGH | HUMAN GROWTH HORMONE (2 PARTS), HYPOPHYSIS SUIS (2 PARTS), HEPAR SUIS (1 PART) | ProBLEN | 78848b52-39f7-4473-ade4-f0eb1ed4a22a | 2016-11-23 | Warnings | 6EC706HI7F |
| Tox-Chord | ALFALFA, ALUMINA, BENZOICUM ACIDUM, CARBONEUM, CETRARIA ISLANDICA, FOLLICULINUM, FUCUS VESICULOSUS, FUMARICUM ACIDUM, HEPAR SUIS, KALI CARBONICUM, KREOSOTUM, NATRUM MURIATICUM, PARAFFINUM, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, PIX LIQUIDA, PLANTAGO MAJOR, PLUMBUM METALLICUM, PULSATILLA (VULGARIS), RADIUM BROMATUM, RESORCINUM, SALOL, SILICEA, SYMPHYTUM OFFICINALE, TABACUM, TEREBINTHINA, THYROIDINUM (BOVINE), TRITICUM REPENS, ZINCUM OXYDATUM | Energetix Corp | 6b0d1628-b20d-426e-9c84-5cceadca3f45 | 2016-11-11 | Warnings | 6EC706HI7F |
| Weight Management Support | ASCLEPIAS VINCETOXICUM, ECHINACEA (ANGUSTIFOLIA), HYPOTHALAMUS (SUIS), CEREBRUM (SUIS), HEPAR SUIS, KIDNEY (SUIS), METHYLCOBALAMIN, PANCREAS SUIS, STOMACH (SUIS), AACG-A, AACG-B, CALCAREA CARBONICA, GAMBOGIA, GELSEMIUM SEMPERVIRENS, GRAPHITES, NUX VOMICA, PHYTOLACCA DECANDRA, 7-KETO (3-ACETYL-7-OXO-DEHYDROEPIANDROSTERONE), ADENOSINUM TRIPHOSPHORICUM DINATRUM, GLUCAGON, INSULINUM, SARCOLACTICUM ACIDUM, PROTEUS (VULGARIS) | Lifetime Fat Loss Centers | 940ca77c-2f80-4457-a31d-08dc70e89805 | 2016-06-23 | Warnings | 6EC706HI7F |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.