Clapiel Detoc Pack Super Lifting Pack
NDC 69977-010
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
Clapiel Detoc Pack Super Lifting Pack is a UNAPPROVED DRUG OTHER-approved product labeled by Aus Korea 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 69977-010 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
69977-010
Proprietary Name:
Clapiel Detoc Pack Super Lifting Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
69977
Product Label ID:
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]
05-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure Chart
Product Details
What is NDC 69977-010?
The NDC code 69977-010 is assigned by the FDA to the product Clapiel Detoc Pack Super Lifting Pack. This pharmaceutical product is labeled by Aus Korea 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: 69977-010-01. 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: 1. Wash your face with soap. (Putting eye cream on your eye rim will be helpful for the dry skin). 2. Open the lid of 'Clapiel Detoc Polymer' and put it into the container of 'Clapiel DETOC Pack'. 3. After strongly shaking for 30 seconds, once again mix them evenly with the pack brush (When completely mixed, the mixed content will turn into a gel-type material). 4. Evenly spread the mixed material with the pack brush; when spreading it, be careful not to put it into your eyes. 5. Do not talk for about 30 minutes and stay comfortably, then the drained skin will be tightened; after spreading the pack, you can make winds by fan, then you will get a feeling of refreshment and may have a better effect (The remained detoc pack material can be applied to the back of your hand/neck). 6. When the DETOC Pack is dried completely, wash off your face once again with soap.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- THIOREDOXIN (UNII: XJZ418133Z)
- THIOREDOXIN (UNII: XJZ418133Z) (Active Moiety)
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:
- WATER (UNII: 059QF0KO0R)
- CAFFEINE (UNII: 3G6A5W338E)
* Please review the full disclaimer at the bottom of this page.
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".
