NDC 63776-454 Relief 3-g12

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63776-454
Proprietary Name:
Relief 3-g12
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Viatrexx Bio Incorporated
Labeler Code:
63776
Start Marketing Date: [9]
07-24-2012
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 63776-454-14

Package Description: 1 BOTTLE, SPRAY in 1 BOX / 30 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 63776-454?

The NDC code 63776-454 is assigned by the FDA to the product Relief 3-g12 which is product labeled by Viatrexx Bio Incorporated. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63776-454-14 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 Relief 3-g12?

This product is used as Acetylcholine chloride Mental clarity Histamine IG support Interferon gamma Immune support Interleukin-12 Immune support Serotonin Neurological support . For symptoms due to sensitivity or reactions.

Which are Relief 3-g12 UNII Codes?

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

Which are Relief 3-g12 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".