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  4. NDC Product Code: 50066-356 Next Day Time Non Drowsy Cold And Flue

NDC 50066-356 Next Day Time Non Drowsy Cold And Flue

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50066-356?
  5. Next Day Time Non Drowsy Cold And Flue 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:
50066-356
Proprietary Name:
Next Day Time Non Drowsy Cold And Flue
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Genomma Lab Usa
Labeler Code:
50066
Product Label ID:
3658b70c-9abf-4c7e-be58-6bcc0d7c78de
Start Marketing Date: [9]
01-19-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
OVAL (C48345)
Size(s):
21 MM
Score:
1

Code Structure Chart

Product Details

What is NDC 50066-356?

The NDC code 50066-356 is assigned by the FDA to the product Next Day Time Non Drowsy Cold And Flue which is product labeled by Genomma Lab Usa. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50066-356-09 10 capsule, liquid filled 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 Next Day Time Non Drowsy Cold And Flue?

■ do not take more than directed (see Warnings)Adults and children 12 years and over: ■ take 2 caplets every 4 hours ■ do not take more than a total of 12 caplets in 24 hoursChildren under 12 years:Do 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 Next Day Time Non Drowsy Cold And Flue UNII Codes?

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

Which are Next Day Time Non Drowsy Cold And Flue 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 Next Day Time Non Drowsy Cold And Flue?

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: 1086997 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / phenylephrine HCl 5 MG Oral Capsule
  • RxCUI: 1086997 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule
  • RxCUI: 1086997 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / phenylephrine hydrochloride 5 MG Oral Capsule

* 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".