83117-003 NDC - BIOGRAM ANTI HAIR LOSS AMPOULE (STEM CELL GERMINAL FLUID)

Drug Information

Product NDC: 83117-003

Proprietary Name: Biogram Anti Hair Loss Ampoule

Non Proprietary Name: Stem Cell Germinal Fluid

Active Ingredient(s):
  • 15 mg/3mL ALLOGENIC ADIPOSE DERIVED MESENCHYMAL STEM CELLS (MSCS) EXOSOMES


Administration Route(s): TOPICAL

Dosage Form(s): POWDER, FOR SOLUTION

Labeler Information

Labeler Name: Beijing Xinghui Regeneration Technology Co., LTD.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:11/20/2022

Package Information

No. Package Code Package Description Billing Unit
183117-003-0220 BOTTLE in 1 BOX (83117-003-02) / 3 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC83117-003The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEBiogram Anti Hair Loss AmpouleThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEStem Cell Germinal FluidThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPOWDER, FOR SOLUTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE11/20/2022This is the date that the labeler indicates was the start of its marketing of the drug 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 NAMEBeijing Xinghui Regeneration Technology Co., LTD.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALLOGENIC ADIPOSE DERIVED MESENCHYMAL STEM CELLS (MSCS) EXOSOMESAn 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 STRENGTH15 
ACTIVE INGRED UNITmg/3mL 

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This page was last updated on: 2/1/2023