Colds and Flu/Multi Symptom Reliever is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by New Sun Inc.. The primary component is Arsenic Trioxide; Baptisia Tinctoria Root; Bryonia Alba Root; Solanum Dulcamara Top; Echinacea, Unspecified; Echinacea Purpurea; Ferrosoferric Phosphate; Gelsemium Sempervirens Root; Potassium Chloride; Phosphorus; Pulsatilla Vulgaris; Sulfur; Zinc Acetate Anhydrous; Zinc Carbonate; Zinc; Zinc Chloride; Zinc Oxide; Zinc Picrate Nonahydrate; Zinc Valerate Dihydrate.
| Product ID | 66579-0090_18089f3e-d601-4140-a539-49256ab77a25 |
| NDC | 66579-0090 |
| Product Type | Human Otc Drug |
| Proprietary Name | Colds and Flu/Multi Symptom Reliever |
| Generic Name | Arsenicum Album, Baptisia Tinctoria, Bryonia, Dulcamara, Echinacea, Echinacea Purpurea, Eupatorium Purpureum, Ferrum Phosphoricum, Gelsemium Sempervirens, Kali Muriaticum, Phosphorus, Pulsatilla, Sulphur, Zincum Aceticum, Zincum Carbonicum, Zincum Metallicum, Zincum Muriaticum, Zincum Oxydatum, Zincum Picricum, Zincum Valerianicum |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-08-20 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | New Sun Inc. |
| Substance Name | ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; SOLANUM DULCAMARA TOP; ECHINACEA, UNSPECIFIED; ECHINACEA PURPUREA; FERROSOFERRIC PHOSPHATE; GELSEMIUM SEMPERVIRENS ROOT; POTASSIUM CHLORIDE; PHOSPHORUS; PULSATILLA VULGARIS; SULFUR; ZINC ACETATE ANHYDROUS; ZINC CARBONATE; ZINC; ZINC CHLORIDE; ZINC OXIDE; ZINC PICRATE NONAHYDRATE; ZINC VALERATE DIHYDRATE |
| Active Ingredient Strength | 10 [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; [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 |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2014-08-20 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-08-20 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| ARSENIC TRIOXIDE | 10 [hp_X]/59mL |
| SPL SET ID: | 0ac6f8e8-b508-40af-b3c5-f866864f10ba |
| Manufacturer | |
| UNII |