NDC 48951-7052-01 - Meteoric Iron Prunus

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
48951-7052
Requested NDC
48951-7052-01
Package NDCs from labels
48951-7052-1, 48951-7052-01
Manufacturer
Uriel Pharmacy Inc.
Effective date
2026-02-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Meteoric Iron PrunusUriel Pharmacy Inc.2026-02-03HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-7052-1Meteoric Iron Prunus10 in 1 BOXLIQUID105
48951-7052-1Meteoric Iron Prunus1 mL in 1 AMPULELIQUID15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7052METEORIC IRON PRUNUS LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20180529_e9020757-2393-4a22-9665-25da0a0993d0.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 10 of 111 · 2,210 matching rows.

Brand, Generic, Manufacturer table
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Reported adverse events (FAERS/openFDA)#

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