NDC 52642-232 Zicam Cold Remedy Soft Chews

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52642-232
Proprietary Name:
Zicam Cold Remedy Soft Chews
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bestco Inc.
Labeler Code:
52642
Start Marketing Date: [9]
04-20-2015
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BROWN (C48332)
Shape:
RECTANGLE (C48347)
Size(s):
20 MM
Imprint(s):
NA
Flavor(s):
CHOCOLATE (C73376)

Product Packages

NDC Code 52642-232-32

Package Description: 32 TABLET, CHEWABLE in 1 CARTON

Product Details

What is NDC 52642-232?

The NDC code 52642-232 is assigned by the FDA to the product Zicam Cold Remedy Soft Chews 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 52642-232-32 32 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 Cold Remedy Soft Chews?

Usesreduces duration of the common coldreduces severity of cold symptoms: sore throat, stuffy nose, sneezing, coughing, nasal congestionhelps restore mental alertness when experiencing fatigue or drowsiness

Which are Zicam Cold Remedy Soft Chews UNII Codes?

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

Which are Zicam Cold Remedy Soft Chews 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".