Home NDC 48951-8351-5 Stannum 5X
Product NDC 48951-8351
Requested package NDC 48951-8351-5
11-digit product format 489518351
Labeler code 48951
Product ID 48951-8351_2c52d67b-abff-a2fa-e063-6294a90a7882
Type HUMAN OTC DRUG
Nonproprietary name Stannum 5X
Dosage form CREAM
Route TOPICAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance TIN
Active strength 5 [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 Stannum 5X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength TIN 5 [hp_X]/g
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 48951-8351-5 Stannum 5X 60 g in 1 TUBE CREAM 60 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-8351 STANNUM 5X CREAM [URIEL PHARMACY INC.] 2 Current NDC, Legacy NDC, 1 package rows 20250124_7a8e2137-c840-37f9-e053-2991aa0ace59.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 48951-8351-5 48951835105 60 g in 1 TUBE (48951-8351-5) 60 g 2009-09-01 0000-00-00 No No Current