NDC 58895-1001 Modlina Peptide Soothing Essential Hydrogel Mask Pack

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:
58895-1001
Proprietary Name:
Modlina Peptide Soothing Essential Hydrogel Mask Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
58895
Start Marketing Date: [9]
08-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 58895-1001?

The NDC code 58895-1001 is assigned by the FDA to the product Modlina Peptide Soothing Essential Hydrogel Mask Pack which is product labeled by Modlina Cosmetics Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 58895-1001-1 25 g 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 Modlina Peptide Soothing Essential Hydrogel Mask Pack?

Clarify the face and tone the skin texture using the toner, peel off the fabric sheet from gel patchgently apply the mask to fit the contours of your face and take off the film of gel patchremove the gel mask hafter 30 minutes later, absorb it with tight tapping and finish

Which are Modlina Peptide Soothing Essential Hydrogel Mask Pack UNII Codes?

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

Which are Modlina Peptide Soothing Essential Hydrogel Mask Pack 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".