NDC 69327-9001 M-rose Seaweed Hydrogel 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:
69327-9001
Proprietary Name:
M-rose Seaweed Hydrogel Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
69327
Start Marketing Date: [9]
10-25-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69327-9001?

The NDC code 69327-9001 is assigned by the FDA to the product M-rose Seaweed Hydrogel Mask which is product labeled by Beauty Line Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69327-9001-2 4 package in 1 box / 25 g in 1 package (69327-9001-1). 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 M-rose Seaweed Hydrogel Mask?

1. First, cleanse your face and apply serum and emulsion. Then place the mask pack over the entire forehead nose to a thickness of about 1 mm.2. Smooth along the jaw line.3. Place over the cheeks and around the mouth. When the mask has completely dried (approximately 15-20 minutes), gently peel off from the chin.4. Press the face with both palms from the center toward the outer edge of the face, pressing the skin lightly.5. With fingertips, press on the areas around the eyes and the mouth, starting from the center of the face and moving outward.

Which are M-rose Seaweed Hydrogel Mask UNII Codes?

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

Which are M-rose Seaweed Hydrogel 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".