Product NDC: | 43742-0135 |
Proprietary Name: | Bronchial Cough |
Non Proprietary Name: | Coccus Cacti, Drosera, Scilla Maritima, Arsenicum Iodatum, Causticum, Cuprum Aceticum, Carbo Vegetabilis |
Active Ingredient(s): | 12; 6; 6; 6; 4; 4; 12; 12; 4 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Coccus Cacti, Drosera, Scilla Maritima, Arsenicum Iodatum, Causticum, Cuprum Aceticum, Carbo Vegetabilis |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43742-0135 |
Labeler Name: | Deseret Biologicals, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120831 |
Package NDC: | 43742-0135-1 |
Package Description: | 30 mL in 1 BOTTLE, DROPPER (43742-0135-1) |
NDC Code | 43742-0135-1 |
Proprietary Name | Bronchial Cough |
Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-0135-1) |
Product NDC | 43742-0135 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Coccus Cacti, Drosera, Scilla Maritima, Arsenicum Iodatum, Causticum, Cuprum Aceticum, Carbo Vegetabilis |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20120831 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Deseret Biologicals, Inc. |
Substance Name | ACTIVATED CHARCOAL; ARSENIC TRIIODIDE; CAUSTICUM; CUPRIC ACETATE; DRIMIA MARITIMA BULB; DROSERA ROTUNDIFOLIA; LACHESIS MUTA VENOM; POTASSIUM CARBONATE; PROTORTONIA CACTI |
Strength Number | 12; 6; 6; 6; 4; 4; 12; 12; 4 |
Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
Pharmaceutical Classes |