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  4. NDC Product Code: 61941-0231 Cold-eeze Plus Nighttime Multi-symptom Relief

NDC 61941-0231 Cold-eeze Plus Nighttime Multi-symptom Relief

View Dosage, Usage, Ingredients, Routes, UNII

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.
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
Labeler Name: [5]
Prophase Labs, Inc.
Labeler Code:
61941
Product Label ID:
176fb319-56bb-4a31-853a-015836113441
Start Marketing Date: [9]
08-15-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
GRAY (C48324)
Shape:
OCTAGON (8 SIDED) (C48344)
Size(s):
15 MM
Imprint(s):
PM
Score:
1
Flavor(s):
BERRY (C73365 - MIXED BERRY)

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 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 61941-0231-8 3 blister pack in 1 carton / 6 tablet, orally disintegrating in 1 blister pack. 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 Nighttime Multi-symptom Relief?

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 Cold-eeze Plus Nighttime Multi-symptom Relief UNII Codes?

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

Which are Cold-eeze Plus Nighttime Multi-symptom 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".