NDC 86052-005 - ODIMOR
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
- 86052-005
- Package NDCs from labels
- 86052-005-01, 86052-005-02
- Manufacturer
- Aquarium Muenster Pahlsmeier GmbH | Merck GKaA
- Effective date
- 2024-04-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| ODIMOR - Aquarium Muenster Pahlsmeier GmbH | Merck GKaA | Aquarium Muenster Pahlsmeier GmbH | Merck GKaA | 2024-04-19 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86052-005-01 | ODIMOR | 20 mL in 1 BOTTLE, GLASS | SOLUTION | 20 | 6 | |
| 86052-005-01 | ODIMOR | 1 in 1 CARTON | SOLUTION | 1 | 6 | |
| 86052-005-02 | ODIMOR | 100 mL in 1 BOTTLE, GLASS | SOLUTION | 100 | 6 | |
| 86052-005-02 | ODIMOR | 1 in 1 CARTON | SOLUTION | 1 | 6 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CUPRIC SULFATE | ACTIVE INGREDIENT | LRX7AJ16DT | ODIMOR (COPPER SULFATE PENTAHYDRATE, MALACHITE GREEN OXALATE) SOLUTION [AQUARIUM MUNSTER PAHLSMEIER GMBH] | 1 | |
| MALACHITE GREEN OXALATE | ACTIVE INGREDIENT | GY1H9O33VU | ODIMOR (COPPER SULFATE PENTAHYDRATE, MALACHITE GREEN OXALATE) SOLUTION [AQUARIUM MUNSTER PAHLSMEIER GMBH] | 1 | |
| CUPRIC CATION | ACTIVE MOIETY | 8CBV67279L | ODIMOR (COPPER SULFATE PENTAHYDRATE, MALACHITE GREEN OXALATE) SOLUTION [AQUARIUM MUNSTER PAHLSMEIER GMBH] | 1 | |
| MALACHITE GREEN CATION | ACTIVE MOIETY | AWT9R95TV1 | ODIMOR (COPPER SULFATE PENTAHYDRATE, MALACHITE GREEN OXALATE) SOLUTION [AQUARIUM MUNSTER PAHLSMEIER GMBH] | 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 |
|---|---|---|---|---|---|---|
| Concept OB | VITAMIN MINERAL SUPPLEMENT | U.S. Pharmaceutical Corporation | 37992a25-68bd-4050-b936-596ddedc25a3 | 2022-11-08 | Warnings, Adverse reactions | LRX7AJ16DT |
| Cuprum Sulphuricum | CUPRUM SULPHURICUM | OHM PHARMA INC. | 7753dbf1-4cce-4a5e-a7d2-549574828268 | 2021-12-30 | Warnings | LRX7AJ16DT |
| Multitrace -4 Pediatric | TRACE ELEMENTS 4 | American Regent, Inc. | 5ee6a685-3c35-467b-8d4d-79efdd0bfa8e | 2019-04-25 | Warnings, Adverse reactions | LRX7AJ16DT |
| Multitrace-5 | TRACE ELEMENTS 5 | American Regent, Inc. | ef63bbe8-ebf8-436c-b38d-6cb92bc91ac0 | 2019-04-25 | Warnings, Adverse reactions | LRX7AJ16DT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.