Meteoric Iron Prunus

Product NDC
48951-7054
11-digit product format
489517054
Labeler code
48951
Product ID
48951-7054_6ad7438d-5aec-d2a5-e053-2991aa0afb52
Type
HUMAN OTC DRUG
Nonproprietary name
Meteoric Iron Prunus
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
SLOE; ECHINACEA, UNSPECIFIED; PHOSPHORUS; IRON; SILICON DIOXIDE
Active strength
2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-7054IInactivated by FDA2026-10-05
excluded packagepackage48951-705448951-7054-3IInactivated by FDA2026-10-05

Reported adverse events (FAERS/openFDA)#

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
910c1bd7-67d1-44c7-ad4f-9445f827edccProduct name120230808

DailyMed Socrata Ingredients#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7054-34895170540360 mL in 1 BOTTLE, DROPPER (48951-7054-3) 60 ml2009-09-010000-00-00NoNoCurrent