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  4. NDC Product Code: 51367-002 Cold Remedy Soothing

NDC 51367-002 Cold Remedy Soothing

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 51367-002?
  5. Cold Remedy Soothing 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:
51367-002
Proprietary Name:
Cold Remedy Soothing
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
International Nature Nutraceuticals
Labeler Code:
51367
Product Label ID:
0e0577fd-e7f7-4772-afce-4e935641b528
Start Marketing Date: [9]
02-24-1987
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Shape:
ROUND (C48348)
Size(s):
11 MM
Score:
1
Flavor(s):
LICORICE (C73397)

Product Packages

NDC Code 51367-002-12

Package Description: 12 TABLET in 1 BOX

Product Details

What is NDC 51367-002?

The NDC code 51367-002 is assigned by the FDA to the product Cold Remedy Soothing which is product labeled by International Nature Nutraceuticals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51367-002-12 12 tablet 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 Cold Remedy Soothing?

Adults and children 12 years of age and olderTake 2 tablets every 4 hours, not to exceed more than 12 tablets in 24 hoursChildren ages 6 to 12 years oldTake 1 tablet every 4 hours, not to exceed more than 6 tablets in 24 hoursChildren under 6 years of ageConsult a doctor

Which are Cold Remedy Soothing UNII Codes?

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

Which are Cold Remedy Soothing 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 Cold Remedy Soothing?

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: 1304074 - chlorpheniramine maleate 1.05 MG / acetaminophen 105 MG Oral Tablet
  • RxCUI: 1304074 - acetaminophen 105 MG / chlorpheniramine maleate 1.05 MG Oral Tablet
  • RxCUI: 1304074 - APAP 105 MG / Chlorpheniramine Maleate 1.05 MG Oral Tablet

* 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".