| Product NDC: | 61941-0217 |
| 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: | 61941-0217 |
| Labeler Name: | ProPhase Labs, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20110801 |
| Package NDC: | 61941-0217-2 |
| Package Description: | 48 BOTTLE, SPRAY in 1 CASE (61941-0217-2) > 22.5 mL in 1 BOTTLE, SPRAY (61941-0217-6) (61941-0217-6) |
| NDC Code | 61941-0217-2 |
| Proprietary Name | Cold-EEZE |
| Package Description | 48 BOTTLE, SPRAY in 1 CASE (61941-0217-2) > 22.5 mL in 1 BOTTLE, SPRAY (61941-0217-6) (61941-0217-6) |
| Product NDC | 61941-0217 |
| 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 |