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 table
LabelManufacturerEffective dateType
ODIMOR - Aquarium Muenster Pahlsmeier GmbH | Merck GKaAAquarium Muenster Pahlsmeier GmbH | Merck GKaA2024-04-19OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86052-005-01ODIMOR20 mL in 1 BOTTLE, GLASSSOLUTION206
86052-005-01ODIMOR1 in 1 CARTONSOLUTION16
86052-005-02ODIMOR100 mL in 1 BOTTLE, GLASSSOLUTION1006
86052-005-02ODIMOR1 in 1 CARTONSOLUTION16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86052-005ODIMOR (COPPER SULFATE PENTAHYDRATE, MALACHITE GREEN OXALATE) SOLUTION [AQUARIUM MUENSTER PAHLSMEIER GMBH]64 package rows20240428_a806954d-caa2-417d-b4d3-2e3775fe1107.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.

Matched openFDA labels page 2 of 2 · 24 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Concept OBVITAMIN MINERAL SUPPLEMENTU.S. Pharmaceutical Corporation37992a25-68bd-4050-b936-596ddedc25a32022-11-08Warnings, Adverse reactionsExact identifier
unii: LRX7AJ16DT
Cuprum SulphuricumCUPRUM SULPHURICUMOHM PHARMA INC.7753dbf1-4cce-4a5e-a7d2-5495748282682021-12-30WarningsExact identifier
unii: LRX7AJ16DT
Multitrace -4 PediatricTRACE ELEMENTS 4American Regent, Inc.5ee6a685-3c35-467b-8d4d-79efdd0bfa8e2019-04-25Warnings, Adverse reactionsExact identifier
unii: LRX7AJ16DT
Multitrace-5TRACE ELEMENTS 5American Regent, Inc.ef63bbe8-ebf8-436c-b38d-6cb92bc91ac02019-04-25Warnings, Adverse reactionsExact identifier
unii: LRX7AJ16DT

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.