Product NDC: | 61727-111 |
Proprietary Name: | Arnica Relief |
Non Proprietary Name: | Arnica Montana 30C |
Active Ingredient(s): | 30 [hp_C]/1 & nbsp; Arnica Montana 30C |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61727-111 |
Labeler Name: | Homeocare Laboratories |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120706 |
Package NDC: | 61727-111-10 |
Package Description: | 100 TABLET in 1 BOTTLE (61727-111-10) |
NDC Code | 61727-111-10 |
Proprietary Name | Arnica Relief |
Package Description | 100 TABLET in 1 BOTTLE (61727-111-10) |
Product NDC | 61727-111 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Arnica Montana 30C |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120706 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Homeocare Laboratories |
Substance Name | ARNICA MONTANA |
Strength Number | 30 |
Strength Unit | [hp_C]/1 |
Pharmaceutical Classes |