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 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
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 48951-8434-3 48951843403 60 mL in 1 BOTTLE, DROPPER (48951-8434-3) 60 ml 2009-09-01 No No Current