Product NDC: | 64762-874 |
Proprietary Name: | NBE Cherry |
Non Proprietary Name: | Zinc Acetate and Zinc Gluconate |
Active Ingredient(s): | 2; 1 [hp_X]/1; [hp_X]/1 & nbsp; Zinc Acetate and Zinc Gluconate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64762-874 |
Labeler Name: | Dynamic Pharmaceuticals Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20101004 |
Package NDC: | 64762-874-25 |
Package Description: | 1 BOTTLE in 1 CARTON (64762-874-25) > 25 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE |
NDC Code | 64762-874-25 |
Proprietary Name | NBE Cherry |
Package Description | 1 BOTTLE in 1 CARTON (64762-874-25) > 25 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE |
Product NDC | 64762-874 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Zinc Acetate and Zinc Gluconate |
Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
Route Name | ORAL |
Start Marketing Date | 20101004 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Dynamic Pharmaceuticals Inc. |
Substance Name | ZINC ACETATE; ZINC GLUCONATE |
Strength Number | 2; 1 |
Strength Unit | [hp_X]/1; [hp_X]/1 |
Pharmaceutical Classes |