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 |