NDC 72371-010 Dermall Matrix Neck Dermal Care 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:
72371-010
Proprietary Name:
Dermall Matrix Neck Dermal Care Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rion Medifab Inc.
Labeler Code:
72371
Start Marketing Date: [9]
05-01-2018
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 72371-010-02

Package Description: 4 POUCH in 1 CARTON / 8 g in 1 POUCH (72371-010-01)

Product Details

What is NDC 72371-010?

The NDC code 72371-010 is assigned by the FDA to the product Dermall Matrix Neck Dermal Care Mask which is product labeled by Rion Medifab Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72371-010-02 4 pouch in 1 carton / 8 g in 1 pouch (72371-010-01). 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 Dermall Matrix Neck Dermal Care Mask?

Directions:1. Soothe your skin with skin lotion after washing neck2. Take off the plastic cover on both sides after opening aluminum pouch.3. Attach biogel sheet to fit your neck4. Take off neck mask after 30~40 minutes.

Which are Dermall Matrix Neck Dermal Care Mask UNII Codes?

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

Which are Dermall Matrix Neck Dermal Care 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".