NDC 72630-020 Dr.plinus Fillincell Multi

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:
72630-020
Proprietary Name:
Dr.plinus Fillincell Multi
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
S Skin Co., Ltd.
Labeler Code:
72630
Start Marketing Date: [9]
05-01-2021
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72630-020-02

Package Description: 2 PATCH in 1 CONTAINER / .3 g in 1 PATCH (72630-020-01)

Product Details

What is NDC 72630-020?

The NDC code 72630-020 is assigned by the FDA to the product Dr.plinus Fillincell Multi which is product labeled by S Skin Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72630-020-02 2 patch in 1 container / .3 g in 1 patch (72630-020-01). 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 Dr.plinus Fillincell Multi?

① Before using the patch, wash your face.② Open the pouch and take the patches out from the clear case, and remove the protective films on patch(* one by one. At this point, be careful not to touch the middle part of the patch.)③ Adjust the patches on your face where you concern and press lightly at a right angle.④ Attach the patch above at least 60 minutes.

Which are Dr.plinus Fillincell Multi UNII Codes?

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

Which are Dr.plinus Fillincell Multi 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".