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  4. NDC Product Code: 64479-401 Cbd Pain Relief Roll On

NDC 64479-401 Cbd Pain Relief Roll On

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64479-401?
  4. Cbd Pain Relief Roll On 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:
64479-401
Proprietary Name:
Cbd Pain Relief Roll On
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Smartscience Laboratories, Inc.
Labeler Code:
64479
Product Label ID:
69a2af68-e202-48f8-8294-47510e3189ff
Start Marketing Date: [9]
02-12-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 64479-401-01

Package Description: 88 mL in 1 BOTTLE, WITH APPLICATOR

Product Details

What is NDC 64479-401?

The NDC code 64479-401 is assigned by the FDA to the product Cbd Pain Relief Roll On which is product labeled by Smartscience Laboratories, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64479-401-01 88 ml in 1 bottle, with applicator . 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 Cbd Pain Relief Roll On?

Use only as directed. Shake well before each use. Roll-on to affected area no more than four times daily. Do not use on children under 12 years of age.

Which are Cbd Pain Relief Roll On UNII Codes?

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

  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
  • MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)

Which are Cbd Pain Relief Roll On 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".