Home NDC 48951-1346 Aurum Stibium
Product NDC 48951-1346
11-digit product format 489511346
Labeler code 48951
Product ID 48951-1346_48871cbc-a3b4-388c-e063-6394a90a3013
Type HUMAN OTC DRUG
Nonproprietary name Aurum Stibium
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ANTIMONY; GOLD
Active strength 8; 10 [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Aurum Stibium
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ANTIMONY 8 [hp_X]/mL GOLD 10 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9IT35J3UV3 Internal UNII lookup 79Y1949PYO 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 48951-1346-1 Aurum Stibium 1 mL in 1 AMPULE LIQUID 1 2 48951-1346-1 Aurum Stibium 10 in 1 BOX LIQUID 10 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-1346 AURUM STIBIUM LIQUID [URIEL PHARMACY INC.] 1 Current NDC, Legacy NDC, 2 package rows 20210312_bd35c88f-c646-4136-e053-2a95a90a0cc1.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 48951-1346-1 48951134601 10 AMPULE in 1 BOX (48951-1346-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current