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Arnicare Procedure Recovery
Arnicare Procedure Recovery - 0220-9050-75 - (ARNICA MONTANA)
Drug Information of Arnicare Procedure Recovery
| Product NDC: | 0220-9050 |
| Proprietary Name: | Arnicare Procedure Recovery |
| Non Proprietary Name: | ARNICA MONTANA |
| Active Ingredient(s): | & nbsp; ARNICA MONTANA |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arnicare Procedure Recovery
| Product NDC: | 0220-9050 |
| Labeler Name: | Laboratoires Boiron |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20071101 |
Package Information of Arnicare Procedure Recovery
| Package NDC: | 0220-9050-75 |
| Package Description: | 1 KIT in 1 PACKAGE (0220-9050-75) * 80 PELLET in 1 TUBE (0220-0508-41) |
NDC Information of Arnicare Procedure Recovery
| NDC Code | 0220-9050-75 |
| Proprietary Name | Arnicare Procedure Recovery |
| Package Description | 1 KIT in 1 PACKAGE (0220-9050-75) * 80 PELLET in 1 TUBE (0220-0508-41) |
| Product NDC | 0220-9050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARNICA MONTANA |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20071101 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Laboratoires Boiron |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |
