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  4. NDC Product Code: 50436-0703 Plus Pharma Pain Reliever,fever Reducer

NDC 50436-0703 Plus Pharma Pain Reliever,fever Reducer

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 50436-0703?
  5. Plus Pharma Pain Reliever,fever Reducer 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:
50436-0703
Proprietary Name:
Plus Pharma Pain Reliever,fever Reducer
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Unit Dose Services
Labeler Code:
50436
Product Label ID:
6717db79-215a-4e14-92e7-4b17b19bcbce
Start Marketing Date: [9]
03-27-2006
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - ROUND)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
GPI;A325
Score:
1

Code Structure Chart

Product Details

What is NDC 50436-0703?

The NDC code 50436-0703 is assigned by the FDA to the product Plus Pharma Pain Reliever,fever Reducer which is product labeled by Unit Dose Services. The product's dosage form is . The product is distributed in a single package with assigned NDC code 50436-0703-1 24 tablet 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 Plus Pharma Pain Reliever,fever Reducer?

Do not take more than directedAGEDOSEAdults and Children 12 years and overTake 2 tablets every 4 to 6 hours while symptoms lastDo not take more than 12 tablets in 24 hoursChildren 6 - 11 yearsTake 1 tablet every 4 to 6 hours while symptoms last Do not take more than 5 tablets in 24 hoursChildren under 6 yearsDo not use adult Regular Strength products in children under 6 years of age; this will provide more than the recommended dose (overdose) of acetaminophen and may cause liver damage.

Which are Plus Pharma Pain Reliever,fever Reducer UNII Codes?

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

Which are Plus Pharma Pain Reliever,fever Reducer 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 Plus Pharma Pain Reliever,fever Reducer?

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:

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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".