NDC 72540-003 Red Ginseng Snail Ferment Mask

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:
72540-003
Proprietary Name:
Red Ginseng Snail Ferment Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Modam Korea
Labeler Code:
72540
Start Marketing Date: [9]
05-08-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72540-003-01

Package Description: 25 mL in 1 PACKAGE

Product Details

What is NDC 72540-003?

The NDC code 72540-003 is assigned by the FDA to the product Red Ginseng Snail Ferment Mask which is product labeled by Modam Korea. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72540-003-01 25 ml in 1 package . 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 Red Ginseng Snail Ferment Mask?

Step 1. Facial forming gelTake an appropriate amount of gel on your palm, make bubbles, apply them to all over the face, gently massage the face, and then rinse the face thoroughly with tepid waterStep 2. Snail ampouleTake an appropriate amount of this product and evenly spread it on the skin.Step 3. Ferment maskAttach this product to the skin for 15-25 minutes and remove the supporter and evenly spread the remaining substances to the skin.

Which are Red Ginseng Snail Ferment Mask UNII Codes?

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

Which are Red Ginseng Snail Ferment Mask 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".