Product NDC: | 61941-0227 |
Proprietary Name: | Cold-EEZE |
Non Proprietary Name: | Zinc Gluconate |
Active Ingredient(s): | 2 [hp_X]/.5mL & nbsp; Zinc Gluconate |
Administration Route(s): | ORAL |
Dosage Form(s): | SPRAY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61941-0227 |
Labeler Name: | ProPhase Labs, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20110801 |
Package NDC: | 61941-0227-2 |
Package Description: | 48 BOTTLE, SPRAY in 1 CASE (61941-0227-2) > 22.5 mL in 1 BOTTLE, SPRAY (61941-0227-6) (61941-0227-6) |
NDC Code | 61941-0227-2 |
Proprietary Name | Cold-EEZE |
Package Description | 48 BOTTLE, SPRAY in 1 CASE (61941-0227-2) > 22.5 mL in 1 BOTTLE, SPRAY (61941-0227-6) (61941-0227-6) |
Product NDC | 61941-0227 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Zinc Gluconate |
Dosage Form Name | SPRAY |
Route Name | ORAL |
Start Marketing Date | 20110801 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | ProPhase Labs, Inc. |
Substance Name | ZINC GLUCONATE |
Strength Number | 2 |
Strength Unit | [hp_X]/.5mL |
Pharmaceutical Classes |