NDC 72695-0011 Medikoii Bio Active Vital Shot Ampoule

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:
72695-0011
Proprietary Name:
Medikoii Bio Active Vital Shot Ampoule
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Theranotics Co.,ltd.
Labeler Code:
72695
Start Marketing Date: [9]
05-01-2020
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72695-0011-2

Package Description: 7 CONTAINER in 1 CARTON / 3 mL in 1 CONTAINER (72695-0011-1)

Product Details

What is NDC 72695-0011?

The NDC code 72695-0011 is assigned by the FDA to the product Medikoii Bio Active Vital Shot Ampoule which is product labeled by Theranotics Co.,ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72695-0011-2 7 container in 1 carton / 3 ml in 1 container (72695-0011-1). 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 Medikoii Bio Active Vital Shot Ampoule?

1) After washing your face, arrange your skin texture with toner.2) Open the product by removing the syringe cap3) Insert the cap into the bottom of syringe and press gently. Make sure you only squeeze out a small amount of ampoule since it is highly concentrated.4) Apply on entire face twice a day.

Which are Medikoii Bio Active Vital Shot Ampoule UNII Codes?

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

Which are Medikoii Bio Active Vital Shot Ampoule 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".