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  4. NDC Product Code: 69842-967 Cvs Maximum Strength Severe Congestion And Cough Overnight Cold And Flu Clear And Cool

NDC 69842-967 Cvs Maximum Strength Severe Congestion And Cough Overnight Cold And Flu Clear And Cool

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69842-967?
  5. Cvs Maximum Strength Severe Congestion And Cough Overnight Cold And Flu Clear And Cool 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:
69842-967
Proprietary Name:
Cvs Maximum Strength Severe Congestion And Cough Overnight Cold And Flu Clear And Cool
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Cvs
Labeler Code:
69842
Product Label ID:
d90ee70c-59df-4976-b66b-b8ece17f744a
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
Flavor(s):
MENTHOL (C73403 - COOLING MENTHOL)

Product Packages

NDC Code 69842-967-12

Package Description: 1 KIT in 1 CARTON * 180 mL in 1 BOTTLE * 180 mL in 1 BOTTLE

Product Details

What is NDC 69842-967?

The NDC code 69842-967 is assigned by the FDA to the product Cvs Maximum Strength Severe Congestion And Cough Overnight Cold And Flu Clear And Cool which is product labeled by Cvs. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69842-967-12 1 kit in 1 carton * 180 ml in 1 bottle * 180 ml in 1 bottle. 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 Cvs Maximum Strength Severe Congestion And Cough Overnight Cold And Flu Clear And Cool?

▪do not take more than 6 doses in any 24-hour period▪measure only with dosing cup provided▪do not use dosing cup with other products▪dose as follows or as directed by a doctor▪mL = milliliter▪adults and children 12 years of age and older: 20 mL in dosing cup provided every 4 hours▪children under 12 years of age: do not use ▪do not take more than directed (see overdose warnings▪do not take more than 4 doses in any 24-hour period▪measure only with dosing cup provided▪do not use dosing cup with other products▪dose as follows or as directed by a doctor▪adults and children 12 years of age and over: 20 ml in dosing cup provided every 4 hours▪children under 12 years of age: do not use

Which are Cvs Maximum Strength Severe Congestion And Cough Overnight Cold And Flu Clear And Cool UNII Codes?

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

Which are Cvs Maximum Strength Severe Congestion And Cough Overnight Cold And Flu Clear And Cool 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 Cvs Maximum Strength Severe Congestion And Cough Overnight Cold And Flu Clear And Cool?

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: 1043543 - dextromethorphan HBr 5 MG / guaiFENesin 100 MG / phenylephrine HCl 2.5 MG in 5 mL Oral Solution
  • RxCUI: 1043543 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML / phenylephrine hydrochloride 0.5 MG/ML Oral Solution
  • RxCUI: 1043543 - dextromethorphan HBr 20 MG / guaifenesin 400 MG / phenylephrine HCl 10 MG per 20 ML Oral Solution
  • RxCUI: 1043543 - dextromethorphan HBr 5 MG / guaifenesin 100 MG / phenylephrine HCl 2.5 MG per 5 ML Oral Solution
  • RxCUI: 2173662 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG / triprolidine HCl 2.5 MG in 20 mL Oral Solution

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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".