| NDC Code | 43742-1435-1 | 
|---|
			| Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-1435-1) | 
|---|
			| Product NDC | 43742-1435 | 
|---|
			| Product Type Name | HUMAN OTC DRUG | 
|---|
			| Proprietary Name | Sinusitx | 
|---|
			
			| Non-Proprietary Name | Plantago Major, Pulsatilla (vulgaris), Luffa Operculata, Mercurius Iodatus Ruber, Mucosa Nasalis Suis, Euphorbium Officinarum, Argentum Nitricum, Hepar Sulphuris Calcareum, Calcarea Carbonica, Natrum Muriaticum, Sinusitisinum | 
|---|
			| Dosage Form | LIQUID | 
|---|
			| Usage | ORAL | 
|---|
			| Start Marketing Date | 20190221 | 
|---|
			| End Marketing Date | 20250707 | 
|---|
			| Marketing Category Name | UNAPPROVED HOMEOPATHIC | 
|---|
			
			| Manufacturer | Deseret Biologicals, Inc. | 
|---|
			| Substance Name | ANEMONE PULSATILLA; CALCIUM SULFIDE; EUPHORBIA RESINIFERA RESIN; LUFFA OPERCULATA FRUIT; MERCURIC IODIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PLANTAGO MAJOR; SILVER NITRATE; SINUSITISINUM; SODIUM CHLORIDE; SUS SCROFA NASAL MUCOSA | 
|---|
			| Strength | 4; 10; 9; 6; 8; 12; 3; 10; 20; 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 | 
|---|