Vaginitis - 50845-0017-1 - (Baptisia tinctoria, Kreosotum, Mercurius iodatus ruber, Mercurius sulphuratus ruber, Nitricum acidum, Platinum metallicum,)

Alphabetical Index


Drug Information of Vaginitis

Product NDC: 50845-0017
Proprietary Name: Vaginitis
Non Proprietary Name: Baptisia tinctoria, Kreosotum, Mercurius iodatus ruber, Mercurius sulphuratus ruber, Nitricum acidum, Platinum metallicum,
Active Ingredient(s): 3; 200; 30; 30; 30; 200; 6; 30    [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL & nbsp;   Baptisia tinctoria, Kreosotum, Mercurius iodatus ruber, Mercurius sulphuratus ruber, Nitricum acidum, Platinum metallicum,
Administration Route(s): ORAL
Dosage Form(s): SPRAY
Coding System: National Drug Codes(NDC)

Labeler Information of Vaginitis

Product NDC: 50845-0017
Labeler Name: Liddell Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date: 20110113

Package Information of Vaginitis

Package NDC: 50845-0017-1
Package Description: 30 mL in 1 BOTTLE, SPRAY (50845-0017-1)

NDC Information of Vaginitis

NDC Code 50845-0017-1
Proprietary Name Vaginitis
Package Description 30 mL in 1 BOTTLE, SPRAY (50845-0017-1)
Product NDC 50845-0017
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Baptisia tinctoria, Kreosotum, Mercurius iodatus ruber, Mercurius sulphuratus ruber, Nitricum acidum, Platinum metallicum,
Dosage Form Name SPRAY
Route Name ORAL
Start Marketing Date 20110113
Marketing Category Name UNAPPROVED HOMEOPATHIC
Labeler Name Liddell Laboratories, Inc.
Substance Name BAPTISIA TINCTORIA ROOT; MERCURIC IODIDE; MERCURIC SULFIDE; NITRIC ACID; PLATINUM; SULFUR IODIDE; SUS SCROFA THYMUS; WOOD CREOSOTE
Strength Number 3; 200; 30; 30; 30; 200; 6; 30
Strength Unit [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL
Pharmaceutical Classes

Complete Information of Vaginitis


General Information