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 |