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  4. NDC Product Code: 61941-0091 Cold-eeze

NDC 61941-0091 Cold-eeze

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61941-0091?
  5. Cold-eeze Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
61941-0091
Proprietary Name:
Cold-eeze
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prophase Labs, Inc.
Labeler Code:
61941
Product Label ID:
58123f25-56d8-4b29-83fd-ca4981a38c08
Start Marketing Date: [9]
02-01-2005
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - SEMI-TRANSLUCENT)
Shape:
OVAL (C48345)
Size(s):
23 MM
Imprint(s):
P
Score:
1
Flavor(s):
CHERRY (C73375 - SUGAR FREE WILD CHERRY)
HONEY (C73394 - SUGAR FREE HONEY LEMON)

Code Structure Chart

Product Details

What is NDC 61941-0091?

The NDC code 61941-0091 is assigned by the FDA to the product Cold-eeze which is product labeled by Prophase Labs, Inc.. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 61941-0091-1 24 package in 1 case / 18 lozenge in 1 package (61941-0091-8), 61941-0091-2 48 package in 1 case / 18 lozenge in 1 package (61941-0091-8), 61941-0091-3 144 package in 1 case / 18 lozenge in 1 package (61941-0091-8). 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?

Adults and children 12 years and overfor best results, begin treatment at start of symptoms (within 24-48 hours of onset)repeat every 2 - 4 hours as needed until all symptoms subsidecompletely dissolve a COLD-EEZE® lozenge in mouth (do not chew)recommended daily dosage is 6 lozenges for adults and 4 lozenges for ages 12-17children under 12 years of age should consult a health professional prior to use

Which are Cold-eeze UNII Codes?

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

Which are Cold-eeze 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:

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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".