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  4. NDC Product Code: 73598-1372 Extra Strength Pain Reliever

NDC 73598-1372 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 73598-1372?
  5. Extra Strength Pain Reliever Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73598-1372
Proprietary Name:
Extra Strength Pain Reliever
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jhk Inc Dba American Safety & First Aid
Labeler Code:
73598
Product Label ID:
87c5ad71-0448-4e0f-acee-bf9a1d38675e
Start Marketing Date: [9]
02-02-2000
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
RECTANGLE (C48347)
Size(s):
18 MM
Imprint(s):
S53
Score:
1

Code Structure Chart

Product Details

What is NDC 73598-1372?

The NDC code 73598-1372 is assigned by the FDA to the product Extra Strength Pain Reliever which is product labeled by Jhk Inc Dba American Safety & First Aid. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73598-1372-1 25 dose pack in 1 box / 2 capsule, coated in 1 dose pack. 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?

2 tablets, with water every 6 hours while symptoms persist; not to exceed 8 tablets in 24 hours or as directed by a doctor. Children under 12 years: consult a doctor.

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:

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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".