Home NDC 53645-1003 Arnica 30X
Product NDC 53645-1003
11-digit product format 536451003
Labeler code 53645
Product ID 53645-1003_1d603875-9235-875e-e063-6394a90ab66c
Type HUMAN OTC DRUG
Nonproprietary name Arnica 30X
Dosage form LIQUID
Route ORAL
Labeler True Botanica, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-08-01
Substance ARNICA MONTANA FLOWER; ARNICA MONTANA ROOT
Active strength 30; 30 [hp_X]/30mL; [hp_X]/30mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Arnica 30X
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ARNICA MONTANA FLOWER 30 [hp_X]/30mL ARNICA MONTANA ROOT 30 [hp_X]/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination OZ0E5Y15PZ Internal UNII lookup MUE8Y11327 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 53645-1003-6 Arnica 30X 30 mL in 1 BOTTLE LIQUID 30 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 53645-1003 ARNICA 30X LIQUID [TRUE BOTANICA, LLC] 1 Current NDC, 1 package rows 20240807_1d603ad7-b839-311d-e063-6294a90add0c.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 53645-1003-6 53645100306 30 mL in 1 BOTTLE (53645-1003-6) 30 ml 2024-08-01 No No Current