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  4. NDC Product Code: 73842-001 Pain Relieving Roll-on Gel

NDC 73842-001 Pain Relieving Roll-on Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 73842-001?
  5. Pain Relieving Roll-on Gel Uses
  6. Active Ingredients UNII Codes
  7. 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:
73842-001
Proprietary Name:
Pain Relieving Roll-on Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Koi Cbd Llc
Labeler Code:
73842
Product Label ID:
a33a18d7-3a97-6609-e053-2995a90a2e87
Start Marketing Date: [9]
04-20-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331 - LIGHT ORANGE)

Product Packages

NDC Code 73842-001-01

Package Description: 89 mL in 1 BOTTLE, WITH APPLICATOR

NDC Code 73842-001-02

Package Description: 534 mL in 1 CASE

Product Details

What is NDC 73842-001?

The NDC code 73842-001 is assigned by the FDA to the product Pain Relieving Roll-on Gel which is product labeled by Koi Cbd Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 73842-001-01 89 ml in 1 bottle, with applicator , 73842-001-02 534 ml in 1 case . 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 Pain Relieving Roll-on Gel?

Uses: For the temporary relief of minor aches and pains of muscles and joints associated with:• backache • arthritis • strains • bruises • sprains

Which are Pain Relieving Roll-on Gel UNII Codes?

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

Which are Pain Relieving Roll-on Gel 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".