NDC 71464-0004 Limulus Bio Cellulose 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:
71464-0004
Proprietary Name:
Limulus Bio Cellulose Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
71464
Start Marketing Date: [9]
06-28-2017
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
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Product Details

What is NDC 71464-0004?

The NDC code 71464-0004 is assigned by the FDA to the product Limulus Bio Cellulose Mask which is product labeled by Skin R&d. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71464-0004-1 1 kit in 1 package * 28 g in 1 pouch (71464-0006-1) * 28 g in 1 pouch (71464-0007-1) * 28 g in 1 pouch (71464-0005-1). 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 Limulus Bio Cellulose Mask?

Open the package and unfold the cellulose mask pack. Then, remove the white film.Attach the product tightly on your face using the side where the white film was removed. Then, remove the fabric on the other side.Carefully adjust the position of the mask on your face. Try not to damage the soft cellulose mask pack.After taking 20-30 minutes of rest, remove the mask. Let your skin absorb the remaining essence with gently dabbing motion.

Which are Limulus Bio Cellulose Mask UNII Codes?

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

Which are Limulus Bio Cellulose 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".