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Gout Control
Gout Control - 51393-7655-2 - (Arnica Montana, Urtica Urens, Silicon Dioxide, and Thuja Occidentalis Root)
Drug Information of Gout Control
| Product NDC: | 51393-7655 |
| Proprietary Name: | Gout Control |
| Non Proprietary Name: | Arnica Montana, Urtica Urens, Silicon Dioxide, and Thuja Occidentalis Root |
| Active Ingredient(s): | 30; 8; 12; 30 [hp_C]/100mL; [hp_X]/1000mL; [hp_X]/1000mL; [hp_C]/100mL & nbsp; Arnica Montana, Urtica Urens, Silicon Dioxide, and Thuja Occidentalis Root |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Gout Control
| Product NDC: | 51393-7655 |
| Labeler Name: | Forces of Nature |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20111201 |
Package Information of Gout Control
| Package NDC: | 51393-7655-2 |
| Package Description: | 33 mL in 1 BOTTLE, DISPENSING (51393-7655-2) |
NDC Information of Gout Control
| NDC Code | 51393-7655-2 |
| Proprietary Name | Gout Control |
| Package Description | 33 mL in 1 BOTTLE, DISPENSING (51393-7655-2) |
| Product NDC | 51393-7655 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Arnica Montana, Urtica Urens, Silicon Dioxide, and Thuja Occidentalis Root |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | TOPICAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Forces of Nature |
| Substance Name | ARNICA MONTANA; SILICON DIOXIDE; THUJA OCCIDENTALIS ROOT; URTICA URENS |
| Strength Number | 30; 8; 12; 30 |
| Strength Unit | [hp_C]/100mL; [hp_X]/1000mL; [hp_X]/1000mL; [hp_C]/100mL |
| Pharmaceutical Classes |
