1. Home
  2. Labeler Index
  3. Prophase Labs, Inc.
  4. NDC Product Code: 61941-0226 Cold-eeze Natural Multi-symptom Relief

NDC 61941-0226 Cold-eeze Natural 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 61941-0226?
  5. Cold-eeze Natural 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:
61941-0226
Proprietary Name:
Cold-eeze Natural 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:
a25b6a72-93b3-487a-9fb9-d33453a448ee
Start Marketing Date: [9]
12-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
OCTAGON (8 SIDED) (C48344)
Size(s):
15 MM
Imprint(s):
ZM
Score:
1
Flavor(s):
LEMON (C73396 - HONEY LEMON)

Code Structure Chart

Product Details

What is NDC 61941-0226?

The NDC code 61941-0226 is assigned by the FDA to the product Cold-eeze Natural Multi-symptom Relief which is product labeled by Prophase Labs, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 61941-0226-5 36 box in 1 case / 4 blister pack in 1 box (61941-0226-4) / 6 tablet, orally disintegrating in 1 blister pack (61941-0226-1), 61941-0226-6 48 box in 1 case / 4 blister pack in 1 box (61941-0226-4) / 6 tablet, orally disintegrating in 1 blister pack (61941-0226-1). 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 Multi-symptom Relief?

Take Cold-EEZE® Plus Multi-Symptom Relief Cold & Flu QuickMelts® when you have cold or flu symptomsAdults: Dissolve entire tablet in mouth. Do not chew. Do not swallow wholeTake 1 tablet 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 6 tablets for adults and 4 tablets for ages 12-17 yearsFor children under 12 years of age, consult a healthcare practitioner before use

Which are Cold-eeze Natural Multi-symptom Relief UNII Codes?

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

Which are Cold-eeze Natural 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:

* Please review the disclaimer below.

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".