NDC 72211-008 Pepplus Special Skin Care Lifting Program

Copper Tripeptide-1,Nicotinoyl Dipeptide-230,Sh-polypeptide-10,Hexapeptide-67 - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
72211-008
Proprietary Name:
Pepplus Special Skin Care Lifting Program
Non-Proprietary Name: [1]
Copper Tripeptide-1, Nicotinoyl Dipeptide-230, Sh-polypeptide-10, Hexapeptide-67 Palmitate, Camellia Sinensis Leaf Extract
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Kit - A packaged collection of related material.
Labeler Name: [5]
Picobio Co., Ltd.
Labeler Code:
72211
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]
11-02-2021
Listing Expiration Date: [11]
12-31-2024
Exclude Flag: [12]
N
Code Structure:
Code Navigator:

Product Packages

NDC Code 72211-008-01

Package Description: 1 KIT in 1 BOX * 8 mL in 1 PACKAGE (72211-006-01) * 1 mL in 1 VIAL (72211-007-01)

Product Details

What is NDC 72211-008?

The NDC code 72211-008 is assigned by the FDA to the product Pepplus Special Skin Care Lifting Program which is a human over the counter drug product labeled by Picobio Co., Ltd.. The generic name of Pepplus Special Skin Care Lifting Program is copper tripeptide-1, nicotinoyl dipeptide-230, sh-polypeptide-10, hexapeptide-67 palmitate, camellia sinensis leaf extract. The product's dosage form is kit. The product is distributed in a single package with assigned NDC code 72211-008-01 1 kit in 1 box * 8 ml in 1 package (72211-006-01) * 1 ml in 1 vial (72211-007-01). 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 Pepplus Special Skin Care Lifting Program?

1. Open Lifting up pack until the dotted line. 2. Open Lifting up capsule and mix with Lifting uppack. (try not to spill the liquid content inside) 3. Seal the package of Lifting up pack and strongly shake thepackage more than 10 times to mix two agents well. (turning into gel when mixed enough)4. Apply the content over your face enough with a brush contained inside the package.5. Regardless of individual difference, wait for 15 ~ 20 minutes. (gently fan yourself while waiting)Try not to move or speak. 6. For the first few times, your skin may feel strongly stretched and there is adifference in color change depending on area. (discharge of toxin out of the skin) Feeling of stretching maydiffer by individual skin condition. 7. After using wash your face with warm water and then use soap to cleanse your face once again. 8. Dry your face with a dry towel.

Which are Pepplus Special Skin Care Lifting Program UNII Codes?

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

  • BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V)
  • BASIC FIBROBLAST GROWTH FACTOR (HUMAN) (UNII: S3529G9M9V) (Active Moiety)
  • PREZATIDE COPPER (UNII: 6BJQ43T1I9)
  • PREZATIDE COPPER (UNII: 6BJQ43T1I9) (Active Moiety)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0)
  • GREEN TEA LEAF (UNII: W2ZU1RY8B0) (Active Moiety)

Which are Pepplus Special Skin Care Lifting Program 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

[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

[3] What kind of product is this? - Indicates 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.

[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 ("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".