81183-101 NDC - THE FLOWER REMEDY PEACEFUL NIGHT (PRUNUS CERASIFERA, CLEMATIS VITALBA, ULMUS PROCERA, IMPATIENS GLANDULIFERA, QUERCUS ROBUR, HELIANTHEMUM NUMMULARIUM, AESCULUS HIPPOCASTANUM, IGNATIA AMARA)

Drug Information

Product NDC: 81183-101

Proprietary Name: THE FLOWER REMEDY Peaceful Night

Non Proprietary Name: Prunus cerasifera, Clematis vitalba, Ulmus procera, Impatiens glandulifera, Quercus robur, Helianthemum nummularium, Aesculus hippocastanum, Ignatia Amara

Active Ingredient(s):
  • 5 [hp_X]/30mL AESCULUS HIPPOCASTANUM FLOWER;
  • 5 [hp_X]/30mL CLEMATIS VITALBA FLOWER;
  • 5 [hp_X]/30mL HELIANTHEMUM NUMMULARIUM FLOWER;
  • 5 [hp_X]/30mL IMPATIENS GLANDULIFERA FLOWER;
  • 5 [hp_X]/30mL PRUNUS CERASIFERA FLOWER;
  • 5 [hp_X]/30mL QUERCUS ROBUR FLOWER;
  • 200 [hp_C]/30mL STRYCHNOS IGNATII SEED;
  • 5 [hp_X]/30mL ULMUS MINOR FLOWERING TWIG


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: The Flower Remedy
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:4/26/2021

Package Information

No. Package Code Package Description Billing Unit
181183-101-3030 mL in 1 BOTTLE, GLASS (81183-101-30)

NDC Record

Field Name Field Value Definition
PRODUCT NDC81183-101The 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 FLOWER REMEDY Peaceful NightThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEPrunus cerasifera, Clematis vitalba, Ulmus procera, Impatiens glandulifera, Quercus robur, Helianthemum nummularium, Aesculus hippocastanum, Ignatia AmaraThe 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 NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/26/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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 NAMEThe Flower RemedyName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAESCULUS HIPPOCASTANUM FLOWER; CLEMATIS VITALBA FLOWER; HELIANTHEMUM NUMMULARIUM FLOWER; IMPATIENS GLANDULIFERA FLOWER; PRUNUS CERASIFERA FLOWER; QUERCUS ROBUR FLOWER; STRYCHNOS IGNATII SEED; ULMUS MINOR FLOWERING TWIGAn 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 STRENGTH5; 5; 5; 5; 5; 5; 200; 5 
ACTIVE INGRED UNIT[hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL 

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