Claritose is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Hello Life, Inc.. The primary component is Onion; Ambrosia Artemisiifolia; Arsenic Trioxide; Arundo Pliniana Root; Arisaema Triphyllum Root; Euphrasia Stricta; Naphthalene; Sodium Chloride; Schoenocaulon Officinale Seed; Wyethia Helenioides Root.
Product ID | 49726-006_7df0b4ca-2f36-e8e5-e053-2991aa0af9ee |
NDC | 49726-006 |
Product Type | Human Otc Drug |
Proprietary Name | Claritose |
Generic Name | Allium Cepa, Ambrosia Artemisiaefolia, Arsenicum Album, Arundo Muritanica, Arum Triphylium, Euphrasia Officinalis, Naphthalinum, Natrum Muriaticum, Sabadilla, Wyethia Heleniodes |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2010-01-07 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Hello Life, Inc. |
Substance Name | ONION; AMBROSIA ARTEMISIIFOLIA; ARSENIC TRIOXIDE; ARUNDO PLINIANA ROOT; ARISAEMA TRIPHYLLUM ROOT; EUPHRASIA STRICTA; NAPHTHALENE; SODIUM CHLORIDE; SCHOENOCAULON OFFICINALE SEED; WYETHIA HELENIOIDES ROOT |
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 |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2010-01-07 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2010-01-07 |
Inactivation Date | 2020-01-31 |
Ingredient | Strength |
---|---|
ONION | 10 [hp_X]/59mL |
SPL SET ID: | 5f2b191e-04a4-4c5a-940e-757cb544c189 |
Manufacturer | |
UNII |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CLARITOSE 78899077 3215878 Live/Registered |
DUOIBES, ALBERT 2006-06-02 |