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  4. NDC Product Code: 66007-101 Zinc Cold Remedy Fast Melting

NDC 66007-101 Zinc Cold Remedy Fast Melting

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66007-101?
  5. Zinc Cold Remedy Fast Melting 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) 66007-101 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:
66007-101
Proprietary Name:
Zinc Cold Remedy Fast Melting
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Izeen Pharma, Inc.
Labeler Code:
66007
Product Label ID:
d17f12ad-6d6c-4a80-a22c-9af2c8d95820
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date: [9]
02-06-2015
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
15 MM
Imprint(s):
CP115
Score:
1
Flavor(s):
CHERRY (C73375)

Code Structure Chart

Product Details

What is NDC 66007-101?

The NDC code 66007-101 is assigned by the FDA to the product Zinc Cold Remedy Fast Melting which is product labeled by Izeen Pharma, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66007-101-25 1 bottle, plastic in 1 carton / 25 tablet 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 Zinc Cold Remedy Fast Melting?

For best results, use at the first sign of a cold and continue to use until symptoms completely subsideadults and children 12 years of age and older:take 1 tablet at the onset of symptomsdissolve entire tablet in mouth. Do not chew. Do not swallow whole.repeat every 4-6 hours, not to exceed 4 tablets in 24 hoursto avoid minor stomach upset, do not take on an empty stomachdo not eat or drink for 15 minutes after use. Do not eat or drink citrus fruits or juices for 30 minutes before or after use. Otherwise, drink plenty of fluids.children under 12 years of age: ask a doctor before use

Which are Zinc Cold Remedy Fast Melting UNII Codes?

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

Which are Zinc Cold Remedy Fast Melting 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".