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  4. NDC Product Code: 64631-7702 Renewal Hgh Advanced

NDC 64631-7702 Renewal Hgh Advanced

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64631-7702?
  4. Renewal Hgh Advanced 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:
64631-7702
Proprietary Name:
Renewal Hgh Advanced
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Always Young, Llc.
Labeler Code:
64631
Product Label ID:
0b0f1aaf-2865-4747-9f07-3b9610960963
Start Marketing Date: [9]
04-23-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 64631-7702?

The NDC code 64631-7702 is assigned by the FDA to the product Renewal Hgh Advanced which is product labeled by Always Young, Llc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64631-7702-1 30 ml in 1 bottle, dropper . 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 Renewal Hgh Advanced?

To temporarily relieve symptoms related to aging; tiredness, weakness, excess fat, wrinkled skin, lack of muscle, etc. To temporarily relieve symptoms related to aging; tiredness, weakness, excess fat, wrinkled skin, lack of muscle, etc.

Which are Renewal Hgh Advanced UNII Codes?

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

Which are Renewal Hgh Advanced 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".