NDC 72543-001 Rayderm Hydrating 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:
72543-001
Proprietary Name:
Rayderm Hydrating Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
72543
Start Marketing Date: [9]
10-11-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
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Product Details

What is NDC 72543-001?

The NDC code 72543-001 is assigned by the FDA to the product Rayderm Hydrating Mask which is product labeled by Vory Medical. Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72543-001-01 24 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 Rayderm Hydrating Mask?

1. After washing your face, apply toner to smooth uneven skin.Tear open the pouch at the top and pull out the sheet mask.2. Unfold the mask and place it onto your face, aligning the holes with your eyes, nose and mouth.3. Remove the sheet mask after relaxing for about 10 - 20 minutes.4. Gently massage the leftover essence into your skin.

Which are Rayderm Hydrating Mask UNII Codes?

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

Which are Rayderm Hydrating 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".