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  4. NDC Product Code: 73045-002 Cbd Unlimited Mistx Topical Analgesic

NDC 73045-002 Cbd Unlimited Mistx Topical Analgesic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73045-002?
  4. Cbd Unlimited Mistx Topical Analgesic 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:
73045-002
Proprietary Name:
Cbd Unlimited Mistx Topical Analgesic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Endexx Corporation
Labeler Code:
73045
Product Label ID:
dec993b7-dda4-4606-aa2f-1135d55874c2
Start Marketing Date: [9]
04-12-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73045-002-30

Package Description: 30 mL in 1 BOTTLE, SPRAY

Product Details

What is NDC 73045-002?

The NDC code 73045-002 is assigned by the FDA to the product Cbd Unlimited Mistx Topical Analgesic which is product labeled by Endexx Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73045-002-30 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 Cbd Unlimited Mistx Topical Analgesic?

Adults and children 12 years of age & older. Spray a thin flim over affected area not more than 3 to 4 times daily: massage not necessary, for children 12 years or younger, consult a doctor.

Which are Cbd Unlimited Mistx Topical Analgesic UNII Codes?

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

Which are Cbd Unlimited Mistx Topical Analgesic 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".