85212-0020 NDC - YVTYVT COPPER PEPTIDES FACIAL SERUM (BETAINE,COPPER TRIPEPTIDE-1,ALLANTOIN,CHRYSANTHELLUM INDICUM WHOLE)

Drug Information

  • Product NDC: 85212-0020
  • Proprietary Name: YVTYVT COPPER PEPTIDES FACIAL SERUM
  • Non Proprietary Name: BETAINE,COPPER TRIPEPTIDE-1,ALLANTOIN,CHRYSANTHELLUM INDICUM WHOLE
  • Active Ingredient(s): .5 g/100mL ALLANTOIN; 5 g/100mL BETAINE; .5 g/100mL CHRYSANTHELLUM INDICUM WHOLE; 1 g/100mL COPPER TRIPEPTIDE-1
  • Administration Route(s): EXTRACORPOREAL
  • Dosage Form(s): CREAM
  • Pharmacy Class(es): Methylating Activity [MoA]; Methylating Agent [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Beijing JUNGE Technology Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: 505G(a)(3)
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:1/10/2025

Package Information

No. Package Code Package Description Billing Unit
185212-0020-125 mL in 1 CAN (85212-0020-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC85212-0020The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PRODUCT TYPE NAMEHUMAN OTC DRUGThis is the date that the labeler indicates was the start of its marketing of the drug product.
PROPRIETARY NAMEYVTYVT COPPER PEPTIDES FACIAL SERUMProduct 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.
NON PROPRIETARY NAMEBETAINE,COPPER TRIPEPTIDE-1,ALLANTOIN,CHRYSANTHELLUM INDICUM WHOLEThis corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
DOSAGE FORM NAMECREAMName of Company corresponding to the labeler code segment of the Product NDC.
ROUTE NAMEEXTRACORPOREALThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/10/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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.
APPLICATION NUMBER505G(a)(3)This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEBeijing JUNGE Technology Co., Ltd.The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
SUBSTANCE NAMEALLANTOIN; BETAINE; CHRYSANTHELLUM INDICUM WHOLE; COPPER TRIPEPTIDE-1An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.5; 5; .5; 1Product 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.
ACTIVE INGRED UNITg/100mL; g/100mL; g/100mL; g/100mL 
PHARM CLASSESMethylating Activity [MoA], Methylating Agent [EPC]The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.

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This page was last updated on: 12/19/2025

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