Home NDC 48951-8356 Stannum 30X
Product NDC 48951-8356
11-digit product format 489518356
Labeler code 48951
Product ID 48951-8356_363833fa-b8d3-1093-e063-6394a90a77fc
Type HUMAN OTC DRUG
Nonproprietary name Stannum 30X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance TIN
Active strength 30 [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 Stannum 30X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TIN 30 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 387GMG9FH5 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 48951-8356-3 Stannum 30X 60 mL in 1 BOTTLE, DROPPER LIQUID 60 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8356 STANNUM 30X LIQUID [URIEL PHARMACY INC.] 2 Current NDC, Legacy NDC, 1 package rows 20210629_9454572b-643c-6cd1-e053-2a95a90ada1a.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 Marketing end Sample Exclude flag Status 48951-8356-3 48951835603 60 mL in 1 BOTTLE, DROPPER (48951-8356-3) 60 ml 2009-09-01 0000-00-00 No No Current