Repiel Smart Foot Peeling Perfect Care
NDC 70758-050

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 70758-050?
  4. Repiel Smart Foot Peeling Perfect Care Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Repiel Smart Foot Peeling Perfect Care is a UNAPPROVED DRUG OTHER-approved product labeled by The Cosrise Co.,ltd. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 70758-050 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
70758-050
Proprietary Name:
Repiel Smart Foot Peeling Perfect Care
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:

Labeler & Regulatory Data

Labeler Name: [5]
The Cosrise Co.,ltd
Labeler Code:
70758
Product Label ID:
1a4a6864-8c1d-4033-ba8d-321ff7a7a022
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.

Marketing Timeline

Start Marketing Date: [9]
05-01-2016
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I

Code Structure Chart

Product Details

What is NDC 70758-050?

The NDC code 70758-050 is assigned by the FDA to the product Repiel Smart Foot Peeling Perfect Care. This pharmaceutical product is labeled by The Cosrise Co.,ltd and is currently categorized as listed product. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 70758-050-02. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Indications & Usage: Get rid of dull and dead skin on the footHow to use: 1. Cut the center line of the Foot peeling mask with scissors after washing the foot. 2. Wear the foot peeling masks on both feet and tight the gloves by sticker strap. 3. Take off the socks after one and half hours. 4. wash the feet gently with water. After 4~5 days, the dirty skin starts to peel off. In 10~14 days, all the rough and dirty foot skin is removed. (Recommendable Use Time: 1.5 hour) *The peeling effect may depend on each person’s condition and please keep the recommendable use hour. It may get the skin hurt in case of excess of the recommendable hour.

Which are the associated UNII Codes?

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

Which are the Inactive Ingredients associated 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:

What is the NDC to RxNorm Crosswalk for this product?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product & Regulatory Definitions
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
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.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".