NDC 60949-110 By Pharmicell Lab Beaucell Dual 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:
60949-110
Proprietary Name:
By Pharmicell Lab Beaucell Dual Hydrogel Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
60949
Start Marketing Date: [9]
10-01-2013
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 60949-110?

The NDC code 60949-110 is assigned by the FDA to the product By Pharmicell Lab Beaucell Dual Hydrogel Mask which is product labeled by Pharmicell Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 60949-110-01 5 patch in 1 carton . 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 By Pharmicell Lab Beaucell Dual Hydrogel Mask?

INDICATIONS AND USAGE:1. After washing your face, apply a toner to clean up your skin.2. Open the pouch and remove both films separating the upper and lower face.3. Attach the transparent film-removed surface of the mask to the skin. (Does not matter which side of mask is adhered onto skin.)4. Remove the mask about 20-40min later, and tap the face lightly for the skin to absorb the contents of the mask remaining on the face.

Which are By Pharmicell Lab Beaucell Dual Hydrogel Mask UNII Codes?

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

Which are By Pharmicell Lab Beaucell Dual 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".