Total FLU-CLD 1 is a Nasal Liquid in the Human Otc Drug category. It is labeled and distributed by White Manufacturing Inc. Dba Micro-west. The primary component is Arsenic Trioxide; Baptisia Tinctoria Root; Bryonia Alba Root; Causticum; Cinchona Officinalis Bark; Solanum Dulcamara Flower; Eupatorium Perfoliatum Flowering Top; Echinacea Purpurea; Eucalyptus Globulus Leaf; Gelsemium Sempervirens Root; Lachesis Muta Venom; Phytolacca Americana Root; Toxicodendron Pubescens Leaf; Lactic Acid, L-; Sulfur; Wyethia Helenioides Root; Influenza A Virus; Cairina Moschata Heart/liver Autolysate.
| Product ID | 61657-0968_ed7f4671-62cf-4f14-891d-71e6bab5eee8 |
| NDC | 61657-0968 |
| Product Type | Human Otc Drug |
| Proprietary Name | Total FLU-CLD 1 |
| Generic Name | Arsenicum Album,sulphur,anas Barbariae,wyethia Helenioides,sarcolacticum Acidum,rhus Toxicodendron,phytolacca Decandra,lachesis Mutus,gelsemium Sempervirens,eucalyptus Globulus,echinacea Purpurea,eupatorium Perfoliatum,dulcamara,,cinchona Officinalis,bryonia Alba,causticum,baptisia Tinctoria, |
| Dosage Form | Liquid |
| Route of Administration | NASAL |
| Marketing Start Date | 2007-03-19 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
| Labeler Name | White Manufacturing Inc. DBA Micro-West |
| Substance Name | ARSENIC TRIOXIDE; BAPTISIA TINCTORIA ROOT; BRYONIA ALBA ROOT; CAUSTICUM; CINCHONA OFFICINALIS BARK; SOLANUM DULCAMARA FLOWER; EUPATORIUM PERFOLIATUM FLOWERING TOP; ECHINACEA PURPUREA; EUCALYPTUS GLOBULUS LEAF; GELSEMIUM SEMPERVIRENS ROOT; LACHESIS MUTA VENOM; PHYTOLACCA AMERICANA ROOT; TOXICODENDRON PUBESCENS LEAF; LACTIC ACID, L-; SULFUR; WYETHIA HELENIOIDES ROOT; INFLUENZA A VIRUS; CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE |
| Active Ingredient Strength | 10 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2018-12-31 |
| Marketing Start Date | 2007-03-19 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | unapproved homeopathic |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2007-03-19 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| ARSENIC TRIOXIDE | 10 [hp_X]/30mL |
| SPL SET ID: | 2cda1532-1007-4afc-b5e1-cfa1f5349190 |
| Manufacturer | |
| UNII |