Home NDC 48951-1214 Apis Belladonna Mercurius
Product NDC 48951-1214
11-digit product format 489511214
Labeler code 48951
Product ID 48951-1214_42f3d7eb-37f8-8755-e063-6294a90ab4b3
Type HUMAN OTC DRUG
Nonproprietary name Apis Belladonna Mercurius
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance APIS MELLIFERA; ATROPA BELLADONNA; MERCURIUS SOLUBILIS
Active strength 5; 4; 17 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Pharmacologic classes Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Apis Belladonna Mercurius
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ATROPA BELLADONNA 5 [hp_X]/mL APIS MELLIFERA 4 [hp_X]/mL MERCURIUS SOLUBILIS 17 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination WQZ3G9PF0H Internal UNII lookup 7S82P3R43Z Internal UNII lookup 324Y4038G2 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 48951-1214-1 Apis Belladonna Mercurius 10 in 1 BOX LIQUID 10 4 48951-1214-1 Apis Belladonna Mercurius 1 mL in 1 AMPULE LIQUID 1 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-1214 APIS BELLADONNA MERCURIUS LIQUID [URIEL PHARMACY INC.] 3 Current NDC, Legacy NDC, 2 package rows 20180411_85c71f6f-3792-4679-aeae-18eaee7db31c.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 48951-1214-1 48951121401 10 AMPULE in 1 BOX (48951-1214-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 0000-00-00 No No Current