NDC 71635-010 Mulbit Firming 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:
71635-010
Proprietary Name:
Mulbit Firming Mask Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
First Cosmetic Co., Ltd
Labeler Code:
71635
Start Marketing Date: [9]
10-01-2017
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 71635-010-02

Package Description: 12 POUCH in 1 CARTON / 23 g in 1 POUCH (71635-010-01)

Product Details

What is NDC 71635-010?

The NDC code 71635-010 is assigned by the FDA to the product Mulbit Firming Mask Pack which is product labeled by First Cosmetic Co., Ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 71635-010-02 12 pouch in 1 carton / 23 g in 1 pouch (71635-010-01). 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 Mulbit Firming Mask Pack?

Directions: 1. After cleansing, dry the face and soothe with toning water. 2. First, gently apply the mask sheet around you eye part and the fit your face contours. 3. Leave it on for 15-20 minutes. 4. Peel off the mask sheet and tab the remaining essence over your face until it completely absorbs to your skin.

Which are Mulbit Firming Mask Pack UNII Codes?

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

Which are Mulbit Firming 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".