Rhumatol Arthitis Symptom and Muscle Pain Relief is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Hello Life, Inc.. The primary component is Actaea Spicata Root; Arnica Montana; Bellis Perennis; Bryonia Alba Root; Oyster Shell Calcium Carbonate, Crude; Calcium Fluoride; Causticum; Black Cohosh; Formic Acid; Hypericum Perforatum; Ledum Palustre Twig; Magnesium Phosphate, Tribasic, Pentahydrate; Phytolacca Americana Root; Pulsatilla Vulgaris; Rhododendron Aureum Leaf; Toxicodendron Pubescens Leaf; Ruta Graveolens Flowering Top; Salicylic Acid; Horse Chestnut; Phosphorus; Lithium Carbonate; Sepia Officinalis Juice; Zinc.
Product ID | 49726-004_7df08284-236b-0914-e053-2991aa0aa0fa |
NDC | 49726-004 |
Product Type | Human Otc Drug |
Proprietary Name | Rhumatol Arthitis Symptom and Muscle Pain Relief |
Generic Name | Actaea Spicata, Aesculus Hippocastanum, Arnica Montana, Bellis Perennis, Bryonia, Calcarea Carbonica, Calcarea Fluorica, Causticum, Cimicifuga Racemosa, Formicum Acidum, Hypericum Perforatum, Ledum Paulstre, Lithium Carbonicum, Magnesia Phosphorica, Phosphorus, Phytolacca Decandra, Pulsatilla, Rhododendron Chrysanthum, Rhus Toxicodendron, Ruta Graveolens, Salicylicum Acidum, Sepia, Zincum Metallicum |
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 | ACTAEA SPICATA ROOT; ARNICA MONTANA; BELLIS PERENNIS; BRYONIA ALBA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; CALCIUM FLUORIDE; CAUSTICUM; BLACK COHOSH; FORMIC ACID; HYPERICUM PERFORATUM; LEDUM PALUSTRE TWIG; MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE; PHYTOLACCA AMERICANA ROOT; PULSATILLA VULGARIS; RHODODENDRON AUREUM LEAF; TOXICODENDRON PUBESCENS LEAF; RUTA GRAVEOLENS FLOWERING TOP; SALICYLIC ACID; HORSE CHESTNUT; PHOSPHORUS; LITHIUM CARBONATE; SEPIA OFFICINALIS JUICE; ZINC |
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; [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 |
---|---|
ACTAEA SPICATA ROOT | 10 [hp_X]/59mL |
SPL SET ID: | 14388c93-bb9f-48f6-a743-f36c6f7e4976 |
Manufacturer | |
UNII |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RHUMATOL 78899057 3398542 Dead/Cancelled |
DUOIBES, ALBERT 2006-06-02 |