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  4. NDC Product Code: 73658-3400 Happy Elf Cbd Pain Relief Cream

NDC 73658-3400 Happy Elf Cbd Pain Relief Cream

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 73658-3400?
  4. Happy Elf Cbd Pain Relief Cream 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:
73658-3400
Proprietary Name:
Happy Elf Cbd Pain Relief Cream
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Happy Elf Cbd Corporation
Labeler Code:
73658
Product Label ID:
40e61bd9-8cf1-420c-9abb-2b2fc7dd650d
Start Marketing Date: [9]
03-19-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 73658-3400?

The NDC code 73658-3400 is assigned by the FDA to the product Happy Elf Cbd Pain Relief Cream which is product labeled by Happy Elf Cbd Corporation. The product's dosage form is . The product is distributed in a single package with assigned NDC code 73658-3400-1 1 tube in 1 package / .114 kg in 1 tube (73658-3400-0). 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 Happy Elf Cbd Pain Relief Cream?

Stop use and ask a doctor if: condition worsens or symptoms persist for more than 7 days, symptoms clear up and occur again within a few days, excessive skin irritation occurs

Which are Happy Elf Cbd Pain Relief Cream UNII Codes?

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

Which are Happy Elf Cbd Pain Relief Cream 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".