Cold-eeze
NDC 61941-0231

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 61941-0231?
  5. Cold-eeze Plus Nighttime Multi-symptom 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.

Cold-eeze is a UNAPPROVED HOMEOPATHIC-approved product labeled by Prophase Labs, Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a gray product. This product entry covers the primary NDC 61941-0231 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
61941-0231
Proprietary Name:
Cold-eeze Plus Nighttime Multi-symptom Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
Prophase Labs, Inc.
Labeler Code:
61941
Product Label ID:
176fb319-56bb-4a31-853a-015836113441
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
08-15-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I

Product Characteristics

Color(s):
GRAY (C48324)
Shape:
OCTAGON (8 SIDED) (C48344)
Size(s):
15 MM
Imprint(s):
PM
Score:
1
Flavor(s):

Code Structure Chart

Product Details

What is NDC 61941-0231?

The NDC code 61941-0231 is assigned by the FDA to the product Cold-eeze Plus Nighttime Multi-symptom Relief. This pharmaceutical product is labeled by Prophase Labs, Inc. and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 61941-0231-8. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Take Cold-EEZE® Plus Nighttime Multi-Symptom Relief Cold & Flu QuickMelts® at night when you have cold or flu symptomsAdults: Dissolve entire tablet in mouth. Do not chew. Do not swallow whole.Take 1 tablet 1 hour before bedtimeDo not eat or drink for 15 minutes after use, otherwise, drink plenty of fluidsRecommended dose is 1 tablet for adultsAllow 6-8 hours for sleep after taking tabletFor individuals under the age of 18, consult a healthcare practitioner before use

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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 & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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".