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  4. NDC Product Code: 55315-531 Extra Strength Pain Reliever

NDC 55315-531 Extra Strength Pain Reliever

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 55315-531?
  5. Extra Strength Pain Reliever 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:
55315-531
Proprietary Name:
Extra Strength Pain Reliever
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Fred's, Inc.
Labeler Code:
55315
Product Label ID:
ae11dd25-c3e5-431c-a4f8-6b081a560fff
Start Marketing Date: [9]
12-11-2005
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
RED (C48326)
Shape:
ROUND (C48348)
Size(s):
11 MM
Imprint(s):
44;531
Score:
1

Code Structure Chart

Product Details

What is NDC 55315-531?

The NDC code 55315-531 is assigned by the FDA to the product Extra Strength Pain Reliever which is product labeled by Fred's, Inc.. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 55315-531-12 1 bottle in 1 carton / 100 tablet in 1 bottle, 55315-531-57 1 bottle in 1 carton / 125 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 Extra Strength Pain Reliever?

Do not take more than directed (see overdose warning)adults and children 12 years and overtake 2 tablets every 4 to 6 hours while symptoms lastdo not take more than 8 tablets in 24 hoursdo not take for more than 10 days unless directed by a doctorchildren under 12 years: do not use this product in children under 12 years of age; this will provide more than the recommended dose (overdose) of acetaminophen and may cause liver damage 

Which are Extra Strength Pain Reliever UNII Codes?

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

Which are Extra Strength Pain Reliever 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 Extra Strength Pain Reliever?

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".