NDC 63029-102 Little Colds Sore Throat Relief Melt Aways

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:
63029-102
Proprietary Name:
Little Colds Sore Throat Relief Melt Aways
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Medtech Products Inc.
Labeler Code:
63029
Start Marketing Date: [9]
12-31-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 63029-102-12

Package Description: 12 GRANULE in 1 CARTON

Product Details

What is NDC 63029-102?

The NDC code 63029-102 is assigned by the FDA to the product Little Colds Sore Throat Relief Melt Aways which is product labeled by Medtech Products Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63029-102-12 12 granule 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 Little Colds Sore Throat Relief Melt Aways?

Empty entire contents of packet onto tongue, allow to dissolve, then swallowFor best taste, do not chew granulesAgeDoseunder 3 yearsConsult a doctor3 to under 6 years1 packet every 2 hours as needed6 years and over1 – 2 packets every 2 hours as needed

Which are Little Colds Sore Throat Relief Melt Aways UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Little Colds Sore Throat Relief Melt Aways?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:

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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".