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  4. NDC Product Code: 58118-5135 Pain Reliever Plus

NDC 58118-5135 Pain Reliever Plus

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 58118-5135?
  5. Pain Reliever Plus 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:
58118-5135
Proprietary Name:
Pain Reliever Plus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Clinical Solutions Wholesale
Labeler Code:
58118
Product Label ID:
17079b90-ccb2-4f35-8641-fdf3613d834f
Start Marketing Date: [9]
11-17-1992
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
13 MM
Imprint(s):
44;159
Score:
1

Code Structure Chart

Product Details

What is NDC 58118-5135?

The NDC code 58118-5135 is assigned by the FDA to the product Pain Reliever Plus which is product labeled by Clinical Solutions Wholesale. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 58118-5135-0 1 tablet, film coated in 1 package , 58118-5135-3 30 tablet, film coated in 1 bottle, plastic , 58118-5135-6 60 tablet, film coated in 1 bottle, plastic , 58118-5135-8 30 tablet, film coated in 1 blister pack , 58118-5135-9 90 tablet, film coated in 1 bottle, plastic . 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 Pain Reliever Plus?

•do not use more than directed•drink a full glass of water with each dose •adults and children 12 years and over •take 2 tablets every 6 hours •do not take more than 8 tablets in 24 hours•children under 12 years: do not use unless directed by a doctor

Which are Pain Reliever Plus UNII Codes?

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

Which are Pain Reliever Plus 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 Pain Reliever Plus?

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: 308297 - acetaminophen 250 MG / aspirin 250 MG / caffeine 65 MG Oral Tablet
  • RxCUI: 308297 - APAP 250 MG / ASA 250 MG / caffeine 65 MG Oral Tablet

* 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".