NDC 70566-040 All In One Dual 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:
70566-040
Proprietary Name:
All In One Dual Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
70566
Start Marketing Date: [9]
02-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 70566-040?

The NDC code 70566-040 is assigned by the FDA to the product All In One Dual Mask which is product labeled by Modecos Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70566-040-01 10 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 All In One Dual Mask?

Indications & Usage: 1. After washing, prepare for mask treatment and tone skin by moisturizing your skin 2. Wear the mask sheet (upper), follow the cutting leave the eyes a space - How to put ear-hold patch- Place the sheet cutting line down. (It can be torn if you pull too much) 3. Take out the mask sheet from the package and remove protecting film. Hold the edges of sheet flat-side up. Pull the sheet gently to both sides along your face line and hook around your ears. 4. Leave the mask 10 to 20 minutes and take it off. 5. Massage and dab the face gently let the essence absorb into skin cell well.

Which are All In One Dual Mask UNII Codes?

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

Which are All In One Dual 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".