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  4. NDC Product Code: 47219-252 Nyloxin Stage 3 Pain Relief

NDC 47219-252 Nyloxin Stage 3 Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 47219-252?
  4. Nyloxin Stage 3 Pain Relief 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:
47219-252
Proprietary Name:
Nyloxin Stage 3 Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Receptopharm Inc
Labeler Code:
47219
Product Label ID:
f2248520-d934-11de-8c20-0002a5d5c51b
Start Marketing Date: [9]
08-25-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 47219-252?

The NDC code 47219-252 is assigned by the FDA to the product Nyloxin Stage 3 Pain Relief which is product labeled by Receptopharm Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 47219-252-10 1 bottle, spray in 1 box / 30 ml in 1 bottle, spray. 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 Nyloxin Stage 3 Pain Relief?

Uses: Temporarily relieves pain associated with sore back, inflamed joints, migraines, painful menses, and general presistent pain

Which are Nyloxin Stage 3 Pain Relief UNII Codes?

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

Which are Nyloxin Stage 3 Pain Relief 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".