Arnicare - 0220-9000-65 - (ARNICA MONTANA)

Alphabetical Index


Drug Information of Arnicare

Product NDC: 0220-9000
Proprietary Name: Arnicare
Non Proprietary Name: ARNICA MONTANA
Active Ingredient(s): 1    [hp_X]/g & nbsp;   ARNICA MONTANA
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of Arnicare

Product NDC: 0220-9000
Labeler Name: Laboratoires Boiron
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20070109

Package Information of Arnicare

Package NDC: 0220-9000-65
Package Description: 1 TUBE in 1 PACKAGE (0220-9000-65) > 14 g in 1 TUBE

NDC Information of Arnicare

NDC Code 0220-9000-65
Proprietary Name Arnicare
Package Description 1 TUBE in 1 PACKAGE (0220-9000-65) > 14 g in 1 TUBE
Product NDC 0220-9000
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ARNICA MONTANA
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20070109
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Laboratoires Boiron
Substance Name ARNICA MONTANA
Strength Number 1
Strength Unit [hp_X]/g
Pharmaceutical Classes

Complete Information of Arnicare


General Information