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NDC 71064-0011 Phuel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 71064-0011?
  4. Active Ingredients UNII Codes
  5. 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:
71064-0011
Proprietary Name:
Phuel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Relion Manufacturing
Labeler Code:
71064
Product Label ID:
c0eb2461-47de-4e0e-e053-2a95a90acf60
Start Marketing Date: [9]
11-07-2018
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71064-0011-7

Package Description: 210 mL in 1 BOTTLE

Product Details

What is NDC 71064-0011?

The NDC code 71064-0011 is assigned by the FDA to the product Phuel which is product labeled by Relion Manufacturing. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71064-0011-7 210 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.

Which are Phuel UNII Codes?

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

  • MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T)
  • MAGNESIUM CATION (UNII: T6V3LHY838) (Active Moiety)

Which are Phuel 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:

* 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".