Cold-EEZE - 61941-0217-2 - (Zinc Gluconate)

Alphabetical Index


Drug Information of Cold-EEZE

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)

Labeler Information of Cold-EEZE

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 Information of Cold-EEZE

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 Information of Cold-EEZE

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

Complete Information of Cold-EEZE


General Information