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  4. NDC Product Code: 69977-010 Clapiel Detoc Pack Super Lifting Pack

NDC 69977-010 Clapiel Detoc Pack Super Lifting Pack

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 69977-010?
  4. Clapiel Detoc Pack Super Lifting Pack Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

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

Get all the details for National Drug Code (NDC) 69977-010 in one place. This page breaks down everything you need to know about the NDC, including proprietary name, active and inactive substances, package configurations, billing units, labeler information, and routes of administration. It also includes enhanced data such as HCPCS codes, FDA product labels with images, UNIIs, and RxNorm cross-references. Whether you're a healthcare professional verifying drug data or a consumer researching medication, this NDC page helps you make informed, accurate decisions.

NDC Product Code:
69977-010
Proprietary Name:
Clapiel Detoc Pack Super Lifting Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Aus Korea Co., Ltd.
Labeler Code:
69977
Product Label ID:
aaf0cc34-783e-4e3a-81fc-6c10c0a9f40f
Marketing Category: [8]
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date: [9]
05-01-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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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 which is product labeled by Aus Korea Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69977-010-01 10 solution 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 Clapiel Detoc Pack Super Lifting Pack?

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 Clapiel Detoc Pack Super Lifting Pack UNII Codes?

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

Which are Clapiel Detoc Pack Super Lifting Pack 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.

[8] 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.

[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, 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".