NDC 47682-758 Medique Coldeeze

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:
47682-758
Proprietary Name:
Medique Coldeeze
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
47682
Start Marketing Date: [9]
03-17-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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)

Code Structure Chart

Product Details

What is NDC 47682-758?

The NDC code 47682-758 is assigned by the FDA to the product Medique Coldeeze which is product labeled by Unifirst-first Aid Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 47682-758-73 25 lozenge in 1 box . 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 Medique Coldeeze?

Take one lozenge at the onset of symptomsdissolve entire lozenge in mouthdo not chewdo not swallow wholedo not eat or drink for 15 minutes after userepeat every 2 - 4 hours until symptoms subsideAdults 18 years and over: do not exceed 6 lozenges per day Children 12 years to under 18 years: do not exceed 4 lozenges per day Children under 12 years: ask a doctor before use

Which are Medique Coldeeze UNII Codes?

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

Which are Medique Coldeeze 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".