NDC 50090-4156 Cold-eeze

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:
50090-4156
Proprietary Name:
Cold-eeze
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
A-s Medication Solutions
Labeler Code:
50090
Start Marketing Date: [9]
05-07-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - SEMI-TRANSLUCENT)
Shape:
OVAL (C48345)
Size(s):
23 MM
Imprint(s):
P
Score:
1
Flavor(s):
CHERRY (C73375)

Product Packages

NDC Code 50090-4156-0

Package Description: 1 BAG in 1 BOX / 18 LOZENGE in 1 BAG

Product Details

What is NDC 50090-4156?

The NDC code 50090-4156 is assigned by the FDA to the product Cold-eeze which is product labeled by A-s Medication Solutions. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50090-4156-0 1 bag in 1 box / 18 lozenge in 1 bag. 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?

Adults and children 12 years and over:•take Cold-EEZE® when you have cold symptoms •completely dissolve a Cold-EEZE® lozenge in mouth (do not chew)•repeat every 2 - 4 hours as needed until all symptoms subside•recommended daily dosage is 6 lozenges for adults and 4 lozenges for ages 12 - 17Children under 12 years of age should consult a healthcare practitioner prior to use

Which are Cold-eeze UNII Codes?

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

Which are Cold-eeze 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".