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