Pibubab Gold Grain Pack
NDC 70567-020
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.
Pibubab Gold Grain Pack is a UNAPPROVED DRUG OTHER-approved product labeled by Khleekorea. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a product. This product entry covers the primary NDC 70567-020 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
70567-020
Proprietary Name:
Pibubab Gold Grain Pack
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Code Navigator:
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
70567
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]
03-02-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure Chart
Product Details
What is NDC 70567-020?
The NDC code 70567-020 is assigned by the FDA to the product Pibubab Gold Grain Pack. This pharmaceutical product is labeled by Khleekorea 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: 70567-020-02. 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: 1. Remove water on your face after washing face. 2. Put the grain pack powder in bowl and add milk or egg or vegetable juice with mineral water. Mix them together fill the pack material gel get thick and emulsified. 3. Apply a pack on entire face not to enter your eyes carefully with brush. 4. Wash your face softly and lightly not to have strong stimulation to face with water or a wet paper towel after 3~5 minutes. Be carefull not to be dried the pack materail gel out on your face. 5. Apply a few of drops of Pibubab Prestige Grain Ample oil on your wet face, after while tap and rub lightly with your palm.
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- SESAME SEED (UNII: 7Y1255HVXR)
- SESAME SEED (UNII: 7Y1255HVXR) (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:
- ADZUKI BEAN (UNII: 31GYU1X0FP)
- BEAN SPROUT (UNII: 9VZY890UEQ)
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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".
