Product NDC: | 43742-0130 |
Proprietary Name: | Sinusitis |
Non Proprietary Name: | Pulsatilla, Plantago Major, Euphorbium Officinarum, Luffa Operculata, Mercurius Iodatus Ruber, Mucosa Nasalis Suis, Argentum Nitricum |
Active Ingredient(s): | 10; 4; 6; 8; 12; 3; 2; 10; 18; 12; 8 [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; [hp_X]/mL; [hp_X]/mL & nbsp; Pulsatilla, Plantago Major, Euphorbium Officinarum, Luffa Operculata, Mercurius Iodatus Ruber, Mucosa Nasalis Suis, Argentum Nitricum |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 43742-0130 |
Labeler Name: | Deseret Biologicals, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20120906 |
Package NDC: | 43742-0130-1 |
Package Description: | 30 mL in 1 BOTTLE, DROPPER (43742-0130-1) |
NDC Code | 43742-0130-1 |
Proprietary Name | Sinusitis |
Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-0130-1) |
Product NDC | 43742-0130 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Pulsatilla, Plantago Major, Euphorbium Officinarum, Luffa Operculata, Mercurius Iodatus Ruber, Mucosa Nasalis Suis, Argentum Nitricum |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20120906 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Deseret Biologicals, Inc. |
Substance Name | CALCIUM SULFIDE; EUPHORBIA RESINIFERA RESIN; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PLANTAGO MAJOR; PULSATILLA VULGARIS; SILVER NITRATE; SINUSITISINUM; SODIUM CHLORIDE; SUS SCROFA NASAL MUCOSA |
Strength Number | 10; 4; 6; 8; 12; 3; 2; 10; 18; 12; 8 |
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; [hp_X]/mL; [hp_X]/mL |
Pharmaceutical Classes |