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  4. NDC Product Code: 58443-0366 Cbdaf Topical Gel

NDC 58443-0366 Cbdaf Topical Gel

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 58443-0366?
  5. Cbdaf Topical 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:
58443-0366
Proprietary Name:
Cbdaf Topical Gel
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prime Enterprises
Labeler Code:
58443
Product Label ID:
b1940679-80d7-64c2-e053-2995a90ac530
Start Marketing Date: [9]
05-01-2019
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE TO OFF WHITE)

Code Structure Chart

Product Details

What is NDC 58443-0366?

The NDC code 58443-0366 is assigned by the FDA to the product Cbdaf Topical Gel which is product labeled by Prime Enterprises. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58443-0366-3 89 ml in 1 bottle . 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 Cbdaf Topical Gel?

Adults and children over 12 years:apply a thin layer to affected area every 6 to 8 hours, but no more than 3 to 4 times dailyif product comes in contact hands, wash hands with soap and waterchildren 12 years or younger: ask a doctor

Which are Cbdaf Topical Gel UNII Codes?

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

Which are Cbdaf Topical 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".