Home NDC 48951-8434 Sun Pyrite 17X
Product NDC 48951-8434
11-digit product format 489518434
Labeler code 48951
Product ID 48951-8434_3130d5c4-fa48-f6af-e063-6294a90a3708
Type HUMAN OTC DRUG
Nonproprietary name Sun Pyrite 17X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance FERROUS DISULFIDE
Active strength 17 [hp_X]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Additional Listing Data#
Finished product Yes
Brand name base Sun Pyrite 17X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FERROUS DISULFIDE 17 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 132N09W4PR 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 48951-8434-3 Sun Pyrite 17X 60 mL in 1 BOTTLE, DROPPER LIQUID 60 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8434 SUN PYRITE 17X LIQUID [URIEL PHARMACY, INC] 1 Current NDC, 1 package rows 20250327_3130d5c4-fa47-f6af-e063-6294a90a3708.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 48951-8434-3 48951843403 60 mL in 1 BOTTLE, DROPPER (48951-8434-3) 60 ml 2009-09-01 No No Current