Home NDC 48951-8410 Stibium 20X
Product NDC 48951-8410
11-digit product format 489518410
Labeler code 48951
Product ID 48951-8410_4e440513-3fe9-ad73-e063-6294a90a0428
Type HUMAN OTC DRUG
Nonproprietary name Stibium 20X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ANTIMONY
Active strength 20 [hp_X]/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Stibium 20X
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANTIMONY 20 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9IT35J3UV3 Internal UNII lookup
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 48951-8410-3 Stibium 20X 60 mL in 1 BOTTLE, DROPPER LIQUID 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8410 STIBIUM 20X LIQUID [URIEL PHARMACY INC.] 1 Current NDC, 1 package rows 20240319_13f25caf-51f0-6b2f-e063-6394a90a0920.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 48951-8410-3 48951841003 60 mL in 1 BOTTLE, DROPPER (48951-8410-3) 60 ml 2009-09-01 No No Current