NDC 63029-101 Little Remedies Little Colds Mucus Relief Expectorant 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:
63029-101
Proprietary Name:
Little Remedies Little Colds Mucus Relief Expectorant Melt Aways
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
63029
Start Marketing Date: [9]
12-31-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
BUBBLE GUM (C73368)

Code Structure Chart

Product Details

What is NDC 63029-101?

The NDC code 63029-101 is assigned by the FDA to the product Little Remedies Little Colds Mucus Relief Expectorant 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 63029-101-12 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 Remedies Little Colds Mucus Relief Expectorant Melt Aways?

Empty entire contents of packet onto tongue, allow to dissolve, then swallowFor best taste, do not chew granulesDo not take more than 6 doses in any 24-hour periodAgeDoseUnder 4 yearsDo not use4 – under 6 years1 packet every 4 hours6 to under 12 years 1 – 2 packets every 4 hours12 years and over 2 – 4 packets every 4 hours

Which are Little Remedies Little Colds Mucus Relief Expectorant Melt Aways UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Little Remedies Little Colds Mucus Relief Expectorant 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 indicates multiple concept unique identifiers (RXCUIs) are 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".