Home NDC 48951-1384 Arnica Betula B
Product NDC 48951-1384
11-digit product format 489511384
Labeler code 48951
Product ID 48951-1384_49df13d2-5867-7d3a-e063-6394a90a1cc4
Type HUMAN OTC DRUG
Nonproprietary name Arnica Betula B
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance BETULA PUBESCENS LEAF; BETULA PUBESCENS BARK; BOS TAURUS CEREBELLUM; BOS TAURUS BRAIN; BOS TAURUS PINEAL GLAND; SUS SCROFA EAR; BOS TAURUS NERVE; ARNICA MONTANA; LEAD; FORMICA RUFA; BIFENTHRIN; BOS TAURUS MESENCEPHALON; HONEY
Active strength 3; 4; 17; 17; 17; 17; 17; 30; 30; 30; 30; 17; 30 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [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 Arnica Betula B
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BETULA PUBESCENS LEAF 3 [hp_X]/mL BETULA PUBESCENS BARK 4 [hp_X]/mL BOS TAURUS CEREBELLUM 17 [hp_X]/mL BOS TAURUS BRAIN 17 [hp_X]/mL BOS TAURUS PINEAL GLAND 17 [hp_X]/mL SUS SCROFA EAR 17 [hp_X]/mL BOS TAURUS NERVE 17 [hp_X]/mL ARNICA MONTANA 30 [hp_X]/mL LEAD 30 [hp_X]/mL FORMICA RUFA 30 [hp_X]/mL BIFENTHRIN 30 [hp_X]/mL BOS TAURUS MESENCEPHALON 17 [hp_X]/mL HONEY 30 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 13 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 48951-1384-1 Arnica Betula B 10 in 1 BOX LIQUID 10 6 48951-1384-1 Arnica Betula B 1 mL in 1 AMPULE LIQUID 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-1384 ARNICA BETULA B LIQUID [URIEL PHARMACY INC.] 5 Current NDC, 2 package rows 20241218_292c40ab-d670-9dc7-e063-6394a90a992a.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 Sample Exclude flag Status 48951-1384-1 48951138401 10 AMPULE in 1 BOX (48951-1384-1) / 1 mL in 1 AMPULE 10 ampule 2009-09-01 No No Current