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  4. NDC Product Code: 63029-402 Little Colds Decongestant Plus Cough

NDC 63029-402 Little Colds Decongestant Plus Cough

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 63029-402?
  5. Little Colds Decongestant Plus Cough Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63029-402
Proprietary Name:
Little Colds Decongestant Plus Cough
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Medtech Products Inc.
Labeler Code:
63029
Product Label ID:
f49a3ac0-02ba-4c34-bb78-4818c44af91c
Start Marketing Date: [9]
09-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

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

Code Structure Chart

Product Details

What is NDC 63029-402?

The NDC code 63029-402 is assigned by the FDA to the product Little Colds Decongestant Plus Cough 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 63029-402-01 1 bottle, dropper in 1 box / 30 ml in 1 bottle, dropper. 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 Decongestant Plus Cough?

Give this medicine by mouth only. Only use the enclosed dropper. Do not use any other dropper, spoon or dosing device when giving this medicine to your child. Fill the enclosed dropper to the prescribed level and slowly dispense the liquid into your child’s mouth (towards the inner cheek). Do not give more than 6 doses in any 24-hour period (see overdose warning).If needed, repeat dose every 4 hours or as directed by a doctor. Age (yr)DoseUnder 4Do not use4 to under 61 mL6 to under 122 mL

Which are Little Colds Decongestant Plus Cough UNII Codes?

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

Which are Little Colds Decongestant Plus Cough 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:

What is the NDC to RxNorm Crosswalk for Little Colds Decongestant Plus Cough?

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:
  • RxCUI: 1424274 - dextromethorphan HBr 5 MG / phenylephrine HCl 2.5 MG in 1 mL Oral Solution
  • RxCUI: 1424274 - dextromethorphan hydrobromide 5 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Oral Solution
  • RxCUI: 1424274 - dextromethorphan HBr 5 MG / phenylephrine HCl 2.5 MG per 1 ML Oral Solution

* Please review the disclaimer below.

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".