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Arniflora
Arniflora - 53499-5090-1 - (ARNICA MONTANA)
Drug Information of Arniflora
| Product NDC: | 53499-5090 |
| Proprietary Name: | Arniflora |
| Non Proprietary Name: | ARNICA MONTANA |
| Active Ingredient(s): | 1 [hp_X]/28g & nbsp; ARNICA MONTANA |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arniflora
| Product NDC: | 53499-5090 |
| Labeler Name: | Nature's Way Products, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20110101 |
Package Information of Arniflora
| Package NDC: | 53499-5090-1 |
| Package Description: | 1 g in 1 PACKET (53499-5090-1) |
NDC Information of Arniflora
| NDC Code | 53499-5090-1 |
| Proprietary Name | Arniflora |
| Package Description | 1 g in 1 PACKET (53499-5090-1) |
| Product NDC | 53499-5090 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARNICA MONTANA |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110101 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Nature's Way Products, Inc. |
| Substance Name | ARNICA MONTANA |
| Strength Number | 1 |
| Strength Unit | [hp_X]/28g |
| Pharmaceutical Classes |
