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
IngredientStrength
ARNICA MONTANA FLOWER30 [hp_X]/30mL
ARNICA MONTANA ROOT30 [hp_X]/30mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiOZ0E5Y15PZ, MUE8Y11327

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53645-1003-6Arnica 30X30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53645-1003ARNICA 30X LIQUID [TRUE BOTANICA, LLC]1Current NDC, 1 package rows20240807_1d603ad7-b839-311d-e063-6294a90add0c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
53645-1003-65364510030630 mL in 1 BOTTLE (53645-1003-6) 30 ml2024-08-01NoNoCurrent