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  4. NDC Product Code: 57631-116 Relexo Oil

NDC 57631-116 Relexo Oil

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57631-116?
  4. Relexo Oil Uses
  5. Active Ingredients UNII Codes
  6. 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:
57631-116
Proprietary Name:
Relexo Oil
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Invatech Pharma Solutions Llc
Labeler Code:
57631
Product Label ID:
d9c64169-cdcf-40a4-ba1d-7ca924f00d0b
Start Marketing Date: [9]
02-28-2017
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Product Details

What is NDC 57631-116?

The NDC code 57631-116 is assigned by the FDA to the product Relexo Oil which is product labeled by Invatech Pharma Solutions Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57631-116-11 1 bottle in 1 carton / 50 ml 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 Relexo Oil?

This product is used as Natural support for healthy joints. Temporary relieves minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises and sprains.

Which are Relexo Oil UNII Codes?

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

Which are Relexo Oil 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".