1. Home
  2. Labeler Index
  3. Bestco Inc.
  4. NDC Product Code: 52642-231 Zicam Kids Cold Relief Remedy

NDC 52642-231 Zicam Kids Cold Relief Remedy

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52642-231?
  5. Zicam Kids Cold Relief Remedy 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:
52642-231
Proprietary Name:
Zicam Kids Cold Relief Remedy
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bestco Inc.
Labeler Code:
52642
Product Label ID:
2c8815e6-5ac4-21c5-e054-00144ff8d46c
Start Marketing Date: [9]
05-06-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327)
Shape:
RECTANGLE (C48347)
Size(s):
22 MM
Imprint(s):
NA
Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 52642-231-18

Package Description: 18 TABLET, CHEWABLE in 1 CARTON

Product Details

What is NDC 52642-231?

The NDC code 52642-231 is assigned by the FDA to the product Zicam Kids Cold Relief Remedy which is product labeled by Bestco Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 52642-231-18 18 tablet, chewable in 1 carton . 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 Zicam Kids Cold Relief Remedy?

Usestemporarily relieves symptoms of the common coldnasal congestionrunny nosescratchy throat

Which are Zicam Kids Cold Relief Remedy UNII Codes?

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

Which are Zicam Kids Cold Relief Remedy 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".