69977-010 NDC - CLAPIEL DETOC PACK SUPER LIFTING PACK ()

Drug Information

  • Product NDC: 69977-010
  • Proprietary Name: CLAPIEL DETOC PACK SUPER LIFTING PACK
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: AUS KOREA CO., LTD.
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:5/1/2015

Package Information

No. Package Code Package Description Billing Unit
169977-010-0110 SOLUTION in 1 CARTON (69977-010-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC69977-010 
PROPRIETARY NAMECLAPIEL DETOC PACK SUPER LIFTING PACKIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
START MARKETING DATE5/1/2015The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct 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.
LABELER NAMEAUS KOREA CO., LTD.This is the date that the labeler indicates was the start of its marketing of the drug product.

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This page was last updated on: 12/6/2025

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