1. Labeler Index
  2. Sambria Pharmaceuticals Inc.
  3. NDC Product Code: 54723-201 Premium Hemp Pain Relief

NDC 54723-201 Premium Hemp Pain Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

    1. Product Information
    2. Product Packages
    3. What is NDC 54723-201?
    4. Premium Hemp 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:
54723-201
Proprietary Name:
Premium Hemp Pain Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sambria Pharmaceuticals Inc.
Labeler Code:
54723
Product Label ID:
9c1a5a43-6f07-444c-e053-2995a90ab0a0
Start Marketing Date: [9]
01-13-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 54723-201-00

Package Description: 113 g in 1 BOTTLE

Product Details

What is NDC 54723-201?

The NDC code 54723-201 is assigned by the FDA to the product Premium Hemp Pain Relief which is product labeled by Sambria Pharmaceuticals Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 54723-201-00 113 g 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 Premium Hemp Pain Relief?

For adults and children two-years or older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a physician. Apply in a circular motion for 30 to 60 seconds.

Which are Premium Hemp Pain Relief UNII Codes?

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

Which are Premium Hemp 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".