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  4. NDC Product Code: 61941-0234 Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu

NDC 61941-0234 Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61941-0234?
  5. Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu 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.

Get all the details for National Drug Code (NDC) 61941-0234 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
61941-0234
Proprietary Name:
Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prophase Labs, Inc.
Labeler Code:
61941
Product Label ID:
fe58769f-e341-448d-8cab-573aa07d70d8
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
10-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327)
Shape:
OVAL (C48345)
Size(s):
15 MM
Imprint(s):
SMILEY;FACE
Score:
1
Flavor(s):
BERRY (C73365 - MIXED BERRY)

Code Structure Chart

Product Details

What is NDC 61941-0234?

The NDC code 61941-0234 is assigned by the FDA to the product Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu 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 61941-0234-0 36 tablet, orally disintegrating in 1 bottle, plastic . 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 Gummies Plus Multi-symptom Relief Cold And Flu?

Take Cold-EEZE® Plus Multi-Symptom Relief Cold & Flu gummies when you have cold or flu symptomsAdults:Dissolve 2 gummies in mouth. Do not swallow whole. For best results, dissolve in your mouth.Take 2 gummies at the onset of symptomsRepeat every 2-4 hours as needed until all symptoms subsideDo not eat or drink for 15 minutes after use, otherwise, drink plenty of fluidsRecommended daily dose is 12 gummies for adults and 8 gummies for ages 12-17 yearsFor children under 12 years of age, consult a healthcare practitioner before use

Which are Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu UNII Codes?

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

Which are Cold-eeze Gummies Plus Multi-symptom Relief Cold And Flu 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.

[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

[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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".