| NDC Code | 66579-0057-2 |
| Package Description | 29 mL in 1 BOTTLE, SPRAY (66579-0057-2) |
| Product NDC | 66579-0057 |
| Product Type Name | HUMAN OTC DRUG |
| Proprietary Name | Gout Symptom Reliever |
| Non-Proprietary Name | Ammonium Phosphoricum, Belladonna, Colchicum Autumnale, Formicum Acidum, Fraxinus Excelsior, Ledum Palustre, Natrum Carbonicum, Nux Vomica, Urtica Urens |
| Dosage Form | LIQUID |
| Usage | ORAL |
| Start Marketing Date | 20140829 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Manufacturer | New Sun Inc. |
| Substance Name | AMMONIUM PHOSPHATE, DIBASIC; ATROPA BELLADONNA; COLCHICUM AUTUMNALE BULB; FORMIC ACID; FRAXINUS EXCELSIOR BARK; FRAXINUS EXCELSIOR LEAF; LEDUM PALUSTRE TWIG; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; URTICA URENS |
| Strength | 10; 10; 10; 10; 10; 10; 10; 10; 10; 10 |
| Strength Unit | [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL |