Home NDC 48951-7052 Meteoric Iron Prunus
Product NDC 48951-7052
11-digit product format 489517052
Labeler code 48951
Product ID 48951-7052_49ef6475-e616-051b-e063-6394a90a0573
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
Substance ECHINACEA, UNSPECIFIED; IRON; PHOSPHORUS; SILICON DIOXIDE; SLOE
Active strength 3; 12; 6; 12; 2 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Meteoric Iron Prunus
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SLOE 2 [hp_X]/mL ECHINACEA, UNSPECIFIED 3 [hp_X]/mL PHOSPHORUS 6 [hp_X]/mL IRON 12 [hp_X]/mL SILICON DIOXIDE 12 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-7052-1 Meteoric Iron Prunus 10 in 1 BOX LIQUID 10 5 48951-7052-1 Meteoric Iron Prunus 1 mL in 1 AMPULE LIQUID 1 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-7052 METEORIC IRON PRUNUS LIQUID [URIEL PHARMACY INC.] 4 Current NDC, Legacy NDC, 2 package rows 20180529_e9020757-2393-4a22-9665-25da0a0993d0.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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 48951-7052-1 48951705201 10 AMPULE in 1 BOX (48951-7052-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current