Home NDC 48951-5027 Gnaphalium Stannum
Product NDC 48951-5027
11-digit product format 489515027
Labeler code 48951
Product ID 48951-5027_5465cb3f-97e2-345f-e063-6294a90a117e
Type HUMAN OTC DRUG
Nonproprietary name Gnaphalium Stannum
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BOS TAURUS CEREBELLUM; BOS TAURUS BRAIN; BOS TAURUS PINEAL GLAND; PSEUDOGNAPHALIUM LUTEOALBUM LEAF; SUS SCROFA EAR; BOS TAURUS NERVE; BIFENTHRIN; TIN
Active strength 17; 17; 17; 17; 17; 17; 20; 20 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
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 Gnaphalium Stannum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BOS TAURUS CEREBELLUM 17 [hp_X]/mL BOS TAURUS BRAIN 17 [hp_X]/mL BOS TAURUS PINEAL GLAND 17 [hp_X]/mL PSEUDOGNAPHALIUM LUTEOALBUM LEAF 17 [hp_X]/mL SUS SCROFA EAR 17 [hp_X]/mL BOS TAURUS NERVE 17 [hp_X]/mL BIFENTHRIN 20 [hp_X]/mL TIN 20 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 8 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 48951-5027-1 Gnaphalium Stannum 1 mL in 1 AMPULE LIQUID 1 3 48951-5027-1 Gnaphalium Stannum 10 in 1 BOX LIQUID 10 3
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-5027 GNAPHALIUM STANNUM LIQUID [URIEL PHARMACY INC.] 3 Current NDC, Legacy NDC, 2 package rows 20180522_86d7c502-859d-4d47-b81a-c0989395a6a9.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 48951-5027-1 48951502701 10 AMPULE in 1 BOX (48951-5027-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current