1. Home
  2. Labeler Index
  3. Hmp Brands, Llc
  4. NDC Product Code: 80875-421 Cbd4 Freeze Pump Vanishing Scent

NDC 80875-421 Cbd4 Freeze Pump Vanishing Scent

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 80875-421?
  4. Cbd4 Freeze Pump Vanishing Scent 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:
80875-421
Proprietary Name:
Cbd4 Freeze Pump Vanishing Scent
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Hmp Brands, Llc
Labeler Code:
80875
Product Label ID:
507740f3-17d5-4acd-814e-75f5dcb372a0
Start Marketing Date: [9]
10-29-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 80875-421?

The NDC code 80875-421 is assigned by the FDA to the product Cbd4 Freeze Pump Vanishing Scent which is product labeled by Hmp Brands, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 80875-421-60 60 g in 1 tube . 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 Cbd4 Freeze Pump Vanishing Scent?

Adults and children over 12 years:Apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period.After applying, wash hands with soap and waterChildren 12 years or younger: ask a doctor

Which are Cbd4 Freeze Pump Vanishing Scent UNII Codes?

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

Which are Cbd4 Freeze Pump Vanishing Scent 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:

* Please review the disclaimer below.

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".