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  4. NDC Product Code: 73615-104 Md Science Cannabigerol

NDC 73615-104 Md Science Cannabigerol

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 73615-104?
  5. Md Science Cannabigerol 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:
73615-104
Proprietary Name:
Md Science Cannabigerol
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Md Natural Health Llc
Labeler Code:
73615
Product Label ID:
9dbcf5b8-8e9a-46f1-ba21-a37137813c32
Start Marketing Date: [9]
02-15-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)

Product Packages

NDC Code 73615-104-02

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 59 mL in 1 BOTTLE, PLASTIC

NDC Code 73615-104-04

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 118 mL in 1 BOTTLE, PLASTIC

Product Details

What is NDC 73615-104?

The NDC code 73615-104 is assigned by the FDA to the product Md Science Cannabigerol which is product labeled by Md Natural Health Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 73615-104-02 1 bottle, plastic in 1 box / 59 ml in 1 bottle, plastic, 73615-104-04 1 bottle, plastic in 1 box / 118 ml in 1 bottle, plastic. 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 Md Science Cannabigerol?

Apply desired amount directly to the area to be affected.

Which are Md Science Cannabigerol UNII Codes?

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

Which are Md Science Cannabigerol 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".