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  4. NDC Product Code: 69168-235 Pain Reliefextra Strength Extra Strength

NDC 69168-235 Pain Reliefextra Strength Extra Strength

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69168-235?
  5. Pain Reliefextra Strength Extra Strength 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:
69168-235
Proprietary Name:
Pain Reliefextra Strength Extra Strength
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Allegiant Health
Labeler Code:
69168
Product Label ID:
d72d83b8-54ff-4bc4-b66e-bb10d9913f74
Start Marketing Date: [9]
12-17-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
12 MM
Imprint(s):
AZ235
Score:
1

Product Packages

NDC Code 69168-235-05

Package Description: 50 TABLET in 1 BOTTLE

NDC Code 69168-235-50

Package Description: 50 TABLET in 1 BOTTLE

Product Details

What is NDC 69168-235?

The NDC code 69168-235 is assigned by the FDA to the product Pain Reliefextra Strength Extra Strength which is product labeled by Allegiant Health. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 69168-235-05 50 tablet in 1 bottle , 69168-235-50 50 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 Pain Reliefextra Strength Extra Strength?

■ do not use more than directed (see overdose warning)■ adults and children 12 years and over: take 2 tablets every 6 hours. Do not take more than 8 tablets in 24 hours.■  do not use more than 10 days unless directed by a doctor■ children under 12 years: do not use this product in children under 12 years of age; this will provide more than the recommended dose (overdose) and may cause liver damageOverdose warning: Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Which are Pain Reliefextra Strength Extra Strength UNII Codes?

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

Which are Pain Reliefextra Strength Extra Strength 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 Reliefextra Strength Extra Strength?

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".