NDC 58829-312 - Magna Poultice

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
58829-312
Package NDCs from labels
58829-312-20, 58829-312-07
Manufacturer
FIRST PRIORITY INCORPORATED
Effective date
2024-10-28
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Magna Poultice - FIRST PRIORITY INCORPORATEDFIRST PRIORITY INCORPORATED2024-10-28OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58829-312-07Magna Poultice4536 g in 1 PAILPOULTICE45366
58829-312-20Magna Poultice567.0 g in 1 JARPOULTICE567.06
58829-312-20Magna Poultice12 in 1 CASEPOULTICE126

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58829-312MAGNA POULTICE (MAGNESIUM SULFATE) POULTICE [FIRST PRIORITY INCORPORATED]63 package rows20241030_f864dcb1-e489-4092-ac69-b2b2408527ee.zip

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 32 of 32 · 626 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MAGNESIUM SULFATEMAGNESIUM SULFATE HEPTAHYDRATEGland Pharma Limiteda9e706ac-9c5f-4b14-b277-53dee195ffc62020-07-14Warnings, Adverse reactionsExact identifier
unii: SK47B8698T
Pure-AidCAMPHOR, MENTHOL, METHYL SALICYLATEKareway Product, Inc.6def9da7-e118-fd5c-e053-2991aa0a65d22018-06-05WarningsExact identifier
unii: LAV5U5022Y
Pain ReliefDL-CAMPHOR, L-MENTHOL, METHYL SALICYLATE PATCHKareway Product, Inc.d3ede306-9ef7-4a89-896b-c083f6e43c852017-12-05WarningsExact identifier
unii: LAV5U5022Y
Dollar General Medicated Pain Relief PatchCAMPHOR, MENTHOL, METHYL SALICYLATEDOLGENCORP, LLC86b0bd7b-c31c-4c35-a5da-0deac9558abe2017-10-01WarningsExact identifier
unii: LAV5U5022Y
Eagle Brand Medicated Oil AromaticCAMPHOR, MENTHOL, METHYL SALICYLATEBorden Company (Private) Limited54e45d89-e8c3-6fc3-e063-6394a90aac4e2015-06-15WarningsExact identifier
unii: LAV5U5022Y
TIS-U-SOLSODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATEBaxter Healthcare Corporation9da4121f-d62d-4da4-8dfb-0494da16015f2014-02-21Exact identifier
unii: SK47B8698T

Reported adverse events (FAERS/openFDA)#

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