NDC 61941-0223 Cold-eeze Plus Immune Support

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61941-0223
Proprietary Name:
Cold-eeze Plus Immune Support
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
61941
Start Marketing Date: [9]
09-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
OCTAGON (8 SIDED) (C48344)
Size(s):
15 MM
Imprint(s):
ZC
Score:
1
Flavor(s):
ORANGE (C73406 - NATURAL)

Code Structure Chart

Product Details

What is NDC 61941-0223?

The NDC code 61941-0223 is assigned by the FDA to the product Cold-eeze Plus Immune Support which is product labeled by Prophase Labs, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 61941-0223-4 4 blister pack in 1 package / 6 tablet, orally disintegrating in 1 blister pack (61941-0223-1). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Cold-eeze Plus Immune Support?

Take Cold-EEZE® Plus Immune Support QuickMelts® when you have cold symptoms.Adults:Dissolve entire tablet in mouth. Do not chew. Do not swallow whole.Take 1 tablet at the onset of symptoms.Repeat every 2-4 hours as needed until all symptoms subside.Do not eat or drink for 15 minutes after use, otherwise, drink plenty of fluids.Recommended daily dose is 6 tablets for adults.For individuals under the age of 18, consult a healthcare practitioner before use.

Which are Cold-eeze Plus Immune Support UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Cold-eeze Plus Immune Support Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".