Home NDC 48951-4197 Ferrum Quartz
Product NDC 48951-4197
11-digit product format 489514197
Labeler code 48951
Product ID 48951-4197_3b5350ed-8f2f-6acb-e063-6394a90a52ab
Type HUMAN OTC DRUG
Nonproprietary name Ferrum Quartz
Dosage form TABLET
Route ORAL
Labeler Uriel Pharmacy, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2023-03-30
Substance FERROUS SULFATE; SULFUR
Active strength 1; 1 [hp_X]/1; [hp_X]/1
NDC exclude flag No
Listing certified through 2026-12-31
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 Ferrum Quartz
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FERROUS SULFATE 1 [hp_X]/1 SULFUR 1 [hp_X]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 39R4TAN1VT Internal UNII lookup 70FD1KFU70 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 48951-4197-4 Ferrum Quartz 250 in 1 BOTTLE, GLASS TABLET 250 4
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 Sample Exclude flag Status 48951-4197-4 48951419704 250 TABLET in 1 BOTTLE, GLASS (48951-4197-4) 250 tablet 2023-03-30 No No Current