73590-0009 NDC - THE SKINHOUSE ROSE HEAVEN TONER (ROSE EXTRACT, ROSA CANINA FRUIT OIL, PAEONIALACTIFLORA BARK/SAP EXTRACT, LEONTOPODIUM ALPINUM EXTRACT, ADENOSINE, NIACINAMIDE)

Drug Information

Product NDC: 73590-0009

Proprietary Name: THE SKINHOUSE Rose Heaven Toner

Non Proprietary Name: Rose Extract, Rosa Canina Fruit Oil, PaeoniaLactiflora Bark/Sap Extract, Leontopodium Alpinum extract, Adenosine, Niacinamide

Active Ingredient(s):
  • .04 g/100mL ADENOSINE;
  • .1 g/100mL LEONTOPODIUM ALPINUM FLOWER;
  • 2 g/100mL NIACINAMIDE;
  • .1 g/100mL PAEONIA LACTIFLORA WHOLE;
  • .5 g/100mL ROSA CANINA FRUIT;
  • .5 g/100mL ROSA CANINA FRUIT OIL


Administration Route(s): TOPICAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Adenosine Receptor Agonist [EPC];
  • Adenosine Receptor Agonists [MoA]

Labeler Information

Labeler Name: NOKSIBCHO cosmetic Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:3/8/2020

Package Information

No. Package Code Package Description Billing Unit
173590-0009-1130 mL in 1 BOTTLE (73590-0009-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73590-0009The 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 NAMETHE SKINHOUSE Rose Heaven TonerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMERose Extract, Rosa Canina Fruit Oil, PaeoniaLactiflora Bark/Sap Extract, Leontopodium Alpinum extract, Adenosine, NiacinamideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe 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 DATE3/8/2020This 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 NAMENOKSIBCHO cosmetic Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEADENOSINE; LEONTOPODIUM ALPINUM FLOWER; NIACINAMIDE; PAEONIA LACTIFLORA WHOLE; ROSA CANINA FRUIT; ROSA CANINA FRUIT OILAn 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.04; .1; 2; .1; .5; .5 
ACTIVE INGRED UNITg/100mL; g/100mL; g/100mL; g/100mL; g/100mL; g/100mL 
PHARM CLASSESAdenosine Receptor Agonist [EPC], Adenosine Receptor Agonists [MoA] 

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