NDC 70758-020 Repiel Smart Nail Pack Miracle Butter

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:
70758-020
Proprietary Name:
Repiel Smart Nail Pack Miracle Butter
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
70758
Start Marketing Date: [9]
05-01-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 70758-020?

The NDC code 70758-020 is assigned by the FDA to the product Repiel Smart Nail Pack Miracle Butter 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 70758-020-02 10 pouch in 1 carton / 3 ml in 1 pouch (70758-020-01). 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 Smart Nail Pack Miracle Butter?

Indications & Usage: Provides high nutrients on fingernailsHow to use: 1. Cut the Nail mask sheet separately and wear for each finger. 2. While waiting for 20~30 minutes, the nails becomes glittering and get nutrition. (The fingers are free to move around, to type on notebook, to works on a smart phone while even wearing the nail mask because it fits optimally on the fingers.)

Which are Repiel Smart Nail Pack Miracle Butter UNII Codes?

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

Which are Repiel Smart Nail Pack Miracle Butter 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".