Home NDC 48951-4200 Formica Stibium comp.
Product NDC 48951-4200
11-digit product format 489514200
Labeler code 48951
Product ID 48951-4200_43d0bb0c-2c3b-8959-e063-6294a90ac75f
Type HUMAN OTC DRUG
Nonproprietary name Formica Stibium comp.
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ANTIMONY; FORMICA RUFA; SILICON DIOXIDE; SUS SCROFA LUNG
Active strength 8; 15; 12; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 Formica Stibium comp.
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SUS SCROFA LUNG 8 [hp_X]/mL ANTIMONY 15 [hp_X]/mL SILICON DIOXIDE 12 [hp_X]/mL FORMICA RUFA 6 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
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 48951-4200-3 Formica Stibium comp. 60 mL in 1 BOTTLE, DROPPER LIQUID 60 3
DailyMed Socrata Ingredients# 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 48951-4200-3 48951420003 60 mL in 1 BOTTLE, DROPPER (48951-4200-3) 60 ml 2009-09-01 No No Current