Product NDC: | 64762-862 |
Proprietary Name: | NBB |
Non Proprietary Name: | ZINC OXIDE, ZINC GLUCONATE, AND SAMBUCUS NIGRA FLOWERING TOP |
Active Ingredient(s): | .05; 12.42; .25 mg/mL; mg/mL; mg/mL & nbsp; ZINC OXIDE, ZINC GLUCONATE, AND SAMBUCUS NIGRA FLOWERING TOP |
Administration Route(s): | ORAL |
Dosage Form(s): | SPRAY, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64762-862 |
Labeler Name: | Dynamic Pharmaceuticals Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100601 |
Package NDC: | 64762-862-30 |
Package Description: | 1 BOTTLE, PUMP in 1 CARTON (64762-862-30) > 30 mL in 1 BOTTLE, PUMP |
NDC Code | 64762-862-30 |
Proprietary Name | NBB |
Package Description | 1 BOTTLE, PUMP in 1 CARTON (64762-862-30) > 30 mL in 1 BOTTLE, PUMP |
Product NDC | 64762-862 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ZINC OXIDE, ZINC GLUCONATE, AND SAMBUCUS NIGRA FLOWERING TOP |
Dosage Form Name | SPRAY, METERED |
Route Name | ORAL |
Start Marketing Date | 20100601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Dynamic Pharmaceuticals Inc. |
Substance Name | SAMBUCUS NIGRA FLOWERING TOP; ZINC GLUCONATE; ZINC OXIDE |
Strength Number | .05; 12.42; .25 |
Strength Unit | mg/mL; mg/mL; mg/mL |
Pharmaceutical Classes |