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  4. NDC Product Code: 67510-9156 Multi Sympton Cold Day Night

NDC 67510-9156 Multi Sympton Cold Day Night

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 67510-9156?
  5. Multi Sympton Cold Day Night 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:
67510-9156
Proprietary Name:
Multi Sympton Cold Day Night
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kareway Product, Inc.
Labeler Code:
67510
Product Label ID:
e0b9109f-ffc3-4e91-bc12-421372022d5a
Start Marketing Date: [9]
05-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333 - LIGHT BLUE)
WHITE (C48325 - WHITE)
Shape:
ROUND (C48348)
Size(s):
9 MM
Imprint(s):
MS
Score:
1

Code Structure Chart

Product Details

What is NDC 67510-9156?

The NDC code 67510-9156 is assigned by the FDA to the product Multi Sympton Cold Day Night which is product labeled by Kareway Product, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 67510-9156-0 1 kit in 1 package, combination * 1 blister pack in 1 box (67510-4156-1) / 10 tablet in 1 blister pack * 1 blister pack in 1 box (67510-3156-1) / 10 tablet in 1 blister pack. 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 Multi Sympton Cold Day Night?

Do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 tablets every 4 hoursswallow whole - do not crush, chew or dissolvedo not take more than 12 tablets in 24 hourschildren under 12 yearsDo not use this adult product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damage

Which are Multi Sympton Cold Day Night UNII Codes?

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

Which are Multi Sympton Cold Day Night 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 Multi Sympton Cold Day Night?

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: 1086991 - acetaminophen 325 MG / chlorpheniramine maleate 2 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1086991 - acetaminophen 325 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1086991 - APAP 325 MG / chlorpheniramine maleate 2 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1094538 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1094538 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 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".