Home NDC 48951-8433 Sun Pyrite 8X
Product NDC 48951-8433
11-digit product format 489518433
Labeler code 48951
Product ID 48951-8433_2eae3f2d-b712-0f50-e063-6294a90a8349
Type HUMAN OTC DRUG
Nonproprietary name Sun Pyrite 8X
Dosage form POWDER
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance FERROUS DISULFIDE
Active strength 8 [hp_X]/g
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 8X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength FERROUS DISULFIDE 8 [hp_X]/g
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 48951-8433-4 Sun Pyrite 8X 50 g in 1 BOTTLE POWDER 50 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8433 SUN PYRITE 8X POWDER [URIEL PHARMACY, INC] 1 Current NDC, 1 package rows 20250309_2eae3f2d-b711-0f50-e063-6294a90a8349.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 48951-8433-4 48951843304 50 g in 1 BOTTLE (48951-8433-4) 50 g 2009-09-01 No No Current