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Arnica Relief
Arnica Relief - 61727-112-02 - (ARNICA MONTANA)
Drug Information of Arnica Relief
| Product NDC: | 61727-112 |
| Proprietary Name: | Arnica Relief |
| Non Proprietary Name: | ARNICA MONTANA |
| Active Ingredient(s): | 1 [hp_X]/56.7g & nbsp; ARNICA MONTANA |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arnica Relief
| Product NDC: | 61727-112 |
| Labeler Name: | Homeocare Laboratories |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20120410 |
Package Information of Arnica Relief
| Package NDC: | 61727-112-02 |
| Package Description: | 56.7 g in 1 TUBE (61727-112-02) |
NDC Information of Arnica Relief
| NDC Code | 61727-112-02 |
| Proprietary Name | Arnica Relief |
| Package Description | 56.7 g in 1 TUBE (61727-112-02) |
| Product NDC | 61727-112 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARNICA MONTANA |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120410 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Homeocare Laboratories |
| Substance Name | ARNICA MONTANA |
| Strength Number | 1 |
| Strength Unit | [hp_X]/56.7g |
| Pharmaceutical Classes |
