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  4. NDC Product Code: 70567-010 Pibubab Prestige Grain Ampule

NDC 70567-010 Pibubab Prestige Grain Ampule

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 70567-010?
  4. Pibubab Prestige Grain Ampule 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.
NDC Product Code:
70567-010
Proprietary Name:
Pibubab Prestige Grain Ampule
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Khleekorea
Labeler Code:
70567
Product Label ID:
1e3ed9a2-4910-4121-a042-7facf04bdbcc
Start Marketing Date: [9]
03-02-2016
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
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Product Details

What is NDC 70567-010?

The NDC code 70567-010 is assigned by the FDA to the product Pibubab Prestige Grain Ampule which is product labeled by Khleekorea. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70567-010-01 25 ml 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 Pibubab Prestige Grain Ampule?

Indications & Usage: Softly apply cream along the skin texture and pat gently for better absorption. 1. After washing face or applying the pibubab gold grain pack in the evening and without applying the basic cosmetics, put a few of drops of energy ampule oil on your wet face, after while tap and rub lightly with your palm. 2. For the face, apply outwards and top-down for the neck. 3. It is also recommendable to apply after taking a shower.

Which are Pibubab Prestige Grain Ampule UNII Codes?

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

Which are Pibubab Prestige Grain Ampule 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.

[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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".