NDC 73674-001 Leafpro Cbdmed Oil Fs Qp 3%

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
73674-001
Proprietary Name:
Leafpro Cbdmed Oil Fs Qp 3%
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Leafmed Gmbh
Labeler Code:
73674
Start Marketing Date: [9]
04-01-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 73674-001-01

Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 10 mL in 1 BOTTLE, DROPPER

NDC Code 73674-001-02

Package Description: 1 BOTTLE, DROPPER in 1 CARTON / 30 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 73674-001?

The NDC code 73674-001 is assigned by the FDA to the product Leafpro Cbdmed Oil Fs Qp 3% which is product labeled by Leafmed Gmbh. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 73674-001-01 1 bottle, dropper in 1 carton / 10 ml in 1 bottle, dropper, 73674-001-02 1 bottle, dropper in 1 carton / 30 ml in 1 bottle, dropper. 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 Leafpro Cbdmed Oil Fs Qp 3%?

Shake well before useadults and children 12 years and over: take 1 – 3 drops under your tongue and hold it there for as long as possible before swallowingrepeat procedure if requireddo not exceed the recommended daily dose of 400mg CBD (266 drops)for full therapeutic effect use regularly for a period of at least 4-12 weeks

Which are Leafpro Cbdmed Oil Fs Qp 3% UNII Codes?

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

Which are Leafpro Cbdmed Oil Fs Qp 3% 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".