| 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 |