NDC 62041-290 Cellexosome St

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:
62041-290
Proprietary Name:
Cellexosome St
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Prostemics Co., Ltd.
Labeler Code:
62041
Start Marketing Date: [9]
02-01-2020
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 62041-290-02

Package Description: 5 CONTAINER in 1 CARTON / 3 mL in 1 CONTAINER (62041-290-01)

Product Details

What is NDC 62041-290?

The NDC code 62041-290 is assigned by the FDA to the product Cellexosome St which is product labeled by Prostemics Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 62041-290-02 5 container in 1 carton / 3 ml in 1 container (62041-290-01). 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 Cellexosome St?

Directions:■ Put solvent into the powder ampoule and shake gently enough to dissolve the mixture■ Take proper amount and gently apply onto the skin

Which are Cellexosome St UNII Codes?

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

Which are Cellexosome St 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".