| Product NDC: | 49589-103 |
| Proprietary Name: | IZUNRINSE |
| Non Proprietary Name: | Hydrocotyle asiatica, Echinacea purpurea, and Sambucus Nigra Flower |
| Active Ingredient(s): | .25; .5; 4.25 g/mL; g/mL; g/mL & nbsp; Hydrocotyle asiatica, Echinacea purpurea, and Sambucus Nigra Flower |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | MOUTHWASH |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49589-103 |
| Labeler Name: | Izun Pharmaceuticals Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20091101 |
| Package NDC: | 49589-103-50 |
| Package Description: | 500 mL in 1 BOTTLE (49589-103-50) |
| NDC Code | 49589-103-50 |
| Proprietary Name | IZUNRINSE |
| Package Description | 500 mL in 1 BOTTLE (49589-103-50) |
| Product NDC | 49589-103 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hydrocotyle asiatica, Echinacea purpurea, and Sambucus Nigra Flower |
| Dosage Form Name | MOUTHWASH |
| Route Name | TOPICAL |
| Start Marketing Date | 20091101 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Izun Pharmaceuticals Corporation |
| Substance Name | ECHINACEA PURPUREA; HYDROCOTYLE ASIATICA; SAMBUCUS NIGRA FLOWER |
| Strength Number | .25; .5; 4.25 |
| Strength Unit | g/mL; g/mL; g/mL |
| Pharmaceutical Classes |