NDC 69058-500 Maxclinic Deep And Deeper Meso Change 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:
69058-500
Proprietary Name:
Maxclinic Deep And Deeper Meso Change Ampoule
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
N&b Lab.co.ltd
Labeler Code:
69058
Start Marketing Date: [9]
12-20-2016
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 69058-500-02

Package Description: 4 VIAL in 1 CARTON / 7 mL in 1 VIAL (69058-500-01)

Product Details

What is NDC 69058-500?

The NDC code 69058-500 is assigned by the FDA to the product Maxclinic Deep And Deeper Meso Change Ampoule which is product labeled by N&b Lab.co.ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69058-500-02 4 vial in 1 carton / 7 ml in 1 vial (69058-500-01). 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 Maxclinic Deep And Deeper Meso Change Ampoule?

Directions: Apply appropriate amount (8~10 drops) to a clean face (cleansed and toned skin) and gently spread over skin. * Optimal results are achieved when the ampoule is followed by HYALURONIC Meso Change Roller.

Which are Maxclinic Deep And Deeper Meso Change Ampoule UNII Codes?

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

Which are Maxclinic Deep And Deeper Meso Change 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:

* 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".