Home NDC 55714-9025 Arnica montana
Product NDC 55714-9025
11-digit product format 557149025
Labeler code 55714
Product ID 55714-9025_4b3153f6-656b-b318-e063-6294a90adf7d
Type HUMAN OTC DRUG
Nonproprietary name Arnica montana
Dosage form LIQUID
Route ORAL
Labeler Newton Laboratories, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-03-01
Substance ARNICA MONTANA
Active strength 4 [hp_X]/L
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Arnica montana
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA 4 [hp_X]/L
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 55714-9025-6 Arnica montana 3 L in 1 BOTTLE, GLASS LIQUID 3 1
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 55714-9025-6 55714902506 3 L in 1 BOTTLE, GLASS (55714-9025-6) 3 l 2024-03-01 No No Current