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  4. NDC Product Code: 41190-112 Shoprite Daytime Flu Plus Severe Cold And Cough

NDC 41190-112 Shoprite Daytime Flu Plus Severe Cold And Cough

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 41190-112?
  4. Shoprite Daytime Flu Plus Severe Cold 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:
41190-112
Proprietary Name:
Shoprite Daytime Flu Plus Severe Cold And Cough
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Wakefern Food Corporation
Labeler Code:
41190
Product Label ID:
4aeb7f40-b315-48e4-97dc-237d06d0f2d4
Start Marketing Date: [9]
06-28-2013
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 41190-112-07

Package Description: 5 POWDER, FOR SOLUTION in 1 CARTON

Product Details

What is NDC 41190-112?

The NDC code 41190-112 is assigned by the FDA to the product Shoprite Daytime Flu Plus Severe Cold And Cough which is product labeled by Wakefern Food Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 41190-112-07 5 powder, for solution in 1 carton . 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 Shoprite Daytime Flu Plus Severe Cold And Cough?

Do not use more than directedtake every 4 hours, while symptoms persist. Do not take more than 5 packets in 24 hours unless directed by a doctorAgeDosechildren under 4 years of agedo not usechildren 4 to under 12 years of agedo not use unless directed by a doctoradults and children 12 years of age and overone packetdissolve contents of one packet into 8 oz. hot water: sip while hot. Consume entire drink within 10-15 minutes.if using a microwave, add contents of one packet to 8 oz. of cool water: stir briskly before and after heating. Do not overheat.

Which are Shoprite Daytime Flu Plus Severe Cold And Cough UNII Codes?

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

Which are Shoprite Daytime Flu Plus Severe Cold 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 Shoprite Daytime Flu Plus Severe Cold 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: 1659967 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Granules for Oral Solution
  • RxCUI: 1659967 - acetaminophen 650 MG / dextromethorphan hydrobromide 20 MG / phenylephrine hydrochloride 10 MG Granules for Oral Solution
  • RxCUI: 1659967 - acetaminophen 650 MG / dextromethorphan HBr 20 MG / phenylephrine HCl 10 MG Powder for Oral Solution
  • RxCUI: 1659967 - APAP 650 MG / Dextromethorphan Hydrobromide 20 MG / Phenylephrine Hydrochloride 10 MG Granules for 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".