Arnica - 53645-1000-0 - (Arnica)

Alphabetical Index


Drug Information of Arnica

Product NDC: 53645-1000
Proprietary Name: Arnica
Non Proprietary Name: Arnica
Active Ingredient(s): 6    [hp_X]/50mL & nbsp;   Arnica
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Arnica

Product NDC: 53645-1000
Labeler Name: True Botanica, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20121113

Package Information of Arnica

Package NDC: 53645-1000-0
Package Description: 50 mL in 1 BOTTLE, WITH APPLICATOR (53645-1000-0)

NDC Information of Arnica

NDC Code 53645-1000-0
Proprietary Name Arnica
Package Description 50 mL in 1 BOTTLE, WITH APPLICATOR (53645-1000-0)
Product NDC 53645-1000
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Arnica
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20121113
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name True Botanica, LLC
Substance Name ARNICA MONTANA FLOWER
Strength Number 6
Strength Unit [hp_X]/50mL
Pharmaceutical Classes

Complete Information of Arnica


General Information