NDC 70758-070 Repiel Timeless Redness Shot Bio 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:
70758-070
Proprietary Name:
Repiel Timeless Redness Shot Bio Mask
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
The Cosrise Co.,ltd
Labeler Code:
70758
Start Marketing Date: [9]
05-01-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70758-070-02

Package Description: 5 BOTTLE, PLASTIC in 1 CARTON / 25 mL in 1 BOTTLE, PLASTIC (70758-070-01)

Product Details

What is NDC 70758-070?

The NDC code 70758-070 is assigned by the FDA to the product Repiel Timeless Redness Shot Bio Mask which is product labeled by The Cosrise Co.,ltd. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70758-070-02 5 bottle, plastic in 1 carton / 25 ml in 1 bottle, plastic (70758-070-01). 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 Repiel Timeless Redness Shot Bio Mask?

Indications & Usage: Purifies to soothe skin and reduce the appearance of outbreaks. 1. Wash and cleanse the face to increase the effect of the mask 2. After removing mesh, apply the mask sheet smoothly to your face removing the fabric layer 3. Relax leaving the mask on, After 15~20 minute, peel away mask. Massage gently to maximize the effect of essence

Which are Repiel Timeless Redness Shot Bio Mask UNII Codes?

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

Which are Repiel Timeless Redness Shot Bio 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".