Sinusitis - 57520-0292-1 - (Sinusitis)

Alphabetical Index


Drug Information of Sinusitis

Product NDC: 57520-0292
Proprietary Name: Sinusitis
Non Proprietary Name: Sinusitis
Active Ingredient(s): 10; 4; 6; 8; 12; 3; 2; 10; 12; 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;   Sinusitis
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Sinusitis

Product NDC: 57520-0292
Labeler Name: Apotheca Company
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20100414

Package Information of Sinusitis

Package NDC: 57520-0292-1
Package Description: 30 mL in 1 BOTTLE, DROPPER (57520-0292-1)

NDC Information of Sinusitis

NDC Code 57520-0292-1
Proprietary Name Sinusitis
Package Description 30 mL in 1 BOTTLE, DROPPER (57520-0292-1)
Product NDC 57520-0292
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Sinusitis
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20100414
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Apotheca Company
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; 12; 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

Complete Information of Sinusitis


General Information