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  4. NDC Product Code: 71027-020 Rapid Max Maximum Strength Cool And Clear - Cold, Severe Congestion And Cough

NDC 71027-020 Rapid Max Maximum Strength Cool And Clear - Cold, Severe Congestion And Cough

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71027-020?
  4. Rapid Max Maximum Strength Cool And Clear - Cold, Severe Congestion And Cough Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. 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:
71027-020
Proprietary Name:
Rapid Max Maximum Strength Cool And Clear - Cold, Severe Congestion And Cough
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Kingston Pharma Llc
Labeler Code:
71027
Product Label ID:
23c16cf9-b0c9-475c-8014-fca9a843ff56
Start Marketing Date: [9]
03-01-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 71027-020?

The NDC code 71027-020 is assigned by the FDA to the product Rapid Max Maximum Strength Cool And Clear - Cold, Severe Congestion And Cough which is product labeled by Kingston Pharma Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71027-020-06 1 bottle in 1 carton / 177 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 Rapid Max Maximum Strength Cool And Clear - Cold, Severe Congestion And Cough?

Uses Temporarily relieves these common cold/flu symptoms Minor aches and painsHeadacheSore throatNasal congestionFeverCough due to minor throat and bronchial irritation

Which are Rapid Max Maximum Strength Cool And Clear - Cold, Severe Congestion And Cough UNII Codes?

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

Which are Rapid Max Maximum Strength Cool And Clear - Cold, Severe Congestion And 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 Rapid Max Maximum Strength Cool And Clear - Cold, Severe Congestion And 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: 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

* 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".