Home NDC 48951-1393 Arnica e pl. tota 3X
Product NDC 48951-1393
11-digit product format 489511393
Labeler code 48951
Product ID 48951-1393_2c3f4366-9557-509d-e063-6394a90a17ee
Type HUMAN OTC DRUG
Nonproprietary name Arnica e pl. tota 3X
Dosage form LIQUID
Route ORAL
Labeler Uriel Pharmacy, Inc
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2009-09-01
Substance ARNICA MONTANA
Active strength 3 [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 Arnica e pl. tota 3X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 3 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O80TY208ZW 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 48951-1393-3 Arnica e pl. tota 3X 60 mL in 1 BOTTLE, DROPPER LIQUID 60 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 48951-1393 ARNICA E PL. TOTA 3X LIQUID [URIEL PHARMACY, INC] 1 Current NDC, 1 package rows 20250123_2c3f4366-9556-509d-e063-6394a90a17ee.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 48951-1393-3 48951139303 60 mL in 1 BOTTLE, DROPPER (48951-1393-3) 60 ml 2009-09-01 No No Current