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  4. NDC Product Code: 61941-0229 Cold-eeze Natural Allergy Relief

NDC 61941-0229 Cold-eeze Natural Allergy Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61941-0229?
  5. Cold-eeze Natural Allergy Relief 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:
61941-0229
Proprietary Name:
Cold-eeze Natural Allergy Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prophase Labs, Inc.
Labeler Code:
61941
Product Label ID:
aa3db5f9-cade-4d4f-b928-a619a6813391
Start Marketing Date: [9]
01-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GRAY (C48324)
Shape:
OVAL (C48345)
Size(s):
2 MM
Imprint(s):
ZA
Score:
1

Code Structure Chart

Product Details

What is NDC 61941-0229?

The NDC code 61941-0229 is assigned by the FDA to the product Cold-eeze Natural Allergy Relief 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 61941-0229-4 2 blister pack in 1 box / 10 tablet, delayed release in 1 blister pack (61941-0229-1). 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 Natural Allergy Relief?

Take Cold-EEZE® Natural Allergy Symptom Relief when you have allergy symptomsFor ages 12 years and older: Take 1 caplet with waterRepeat every 8-12 hours as needed until all symptoms subsideDo Not Take more than 3 caplets per dayRecommended daily dose is 2 caplets per dayFor individuals under the age of 12, consult a healthcare practitioner before use

Which are Cold-eeze Natural Allergy Relief UNII Codes?

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

Which are Cold-eeze Natural Allergy Relief 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".