73448-0001 NDC - RECALIBR8 (HYPOPHYSIS SUIS, HYPOTHALAMUS SUIS, ACONITUM NAPELLUS, ALOE, ALUMINA, ANTIMONIUM CRUDUM, APIS MELLIFICA, ARGENTUM NITRICUM, ARNICA MONTANA, ARSENICUM ALBUM, BELLADONNA, BELLIS PERENNIS, BRYONIA (ALBA), CALCAREA FLUORICA, CALENDULA OFFICINALIS, CAUSTICUM, CHAMOMILLA, CHELIDONIUM MAJUS, CISTUS CANADENSIS, CLEMATIS ERECTA, FERRUM PHOSPHORICUM, GAMBOGIA, GRAPHITES, HISTAMINUM HYDROCHLORICUM, HYDRASTIS CANADENSIS, HYDROFLUORICUM ACIDUM, HYPERICUM PERFORATUM, IGNATIA AMARA, IMPATIENS GLANDULIFERA, FLOS,)

Drug Information

Product NDC: 73448-0001

Proprietary Name: Recalibr8

Non Proprietary Name: Hypophysis Suis, Hypothalamus Suis, Aconitum Napellus, Aloe, Alumina, Antimonium Crudum, Apis Mellifica, Argentum Nitricum, Arnica Montana, Arsenicum Album, Belladonna, Bellis Perennis, Bryonia (Alba), Calcarea Fluorica, Calendula Officinalis, Causticum, Chamomilla, Chelidonium Majus, Cistus Canadensis, Clematis Erecta, Ferrum Phosphoricum, Gambogia, Graphites, Histaminum Hydrochloricum, Hydrastis canadensis, Hydrofluoricum Acidum, Hypericum Perforatum, Ignatia amara, Impatiens Glandulifera, Flos,

Active Ingredient(s):
  • 12 [hp_X]/mL ACONITUM NAPELLUS WHOLE;
  • 12 [hp_X]/mL ALLYLTHIOUREA;
  • 12 [hp_X]/mL ALOE;
  • 12 [hp_X]/mL ALUMINUM OXIDE;
  • 12 [hp_X]/mL ANTIMONY TRISULFIDE;
  • 12 [hp_X]/mL APIS MELLIFERA;
  • 12 [hp_X]/mL ARNICA MONTANA WHOLE;
  • 12 [hp_X]/mL ARSENIC TRIOXIDE;
  • 12 [hp_X]/mL ATROPA BELLADONNA;
  • 12 [hp_X]/mL BELLIS PERENNIS WHOLE;
  • 12 [hp_X]/mL BRYONIA ALBA ROOT;
  • 12 [hp_X]/mL CALCIUM FLUORIDE;
  • 12 [hp_X]/mL CALENDULA OFFICINALIS FLOWERING TOP;
  • 12 [hp_X]/mL CAUSTICUM;
  • 12 [hp_X]/mL CHELIDONIUM MAJUS WHOLE;
  • 12 [hp_X]/mL CLEMATIS RECTA FLOWERING TOP;
  • 12 [hp_X]/mL COMFREY ROOT;
  • 12 [hp_X]/mL FERROSOFERRIC PHOSPHATE;
  • 12 [hp_X]/mL GAMBOGE;
  • 12 [hp_X]/mL GOLDENSEAL;
  • 12 [hp_X]/mL GRAPHITE;
  • 12 [hp_X]/mL HELIANTHEMUM CANADENSE;
  • 12 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE;
  • 12 [hp_X]/mL HYDROFLUORIC ACID;
  • 12 [hp_X]/mL HYPERICUM PERFORATUM WHOLE;
  • 12 [hp_X]/mL IMPATIENS GLANDULIFERA FLOWER;
  • 12 [hp_X]/mL LACHESIS MUTA VENOM;
  • 12 [hp_X]/mL LEAD;
  • 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE;
  • 12 [hp_X]/mL MATRICARIA CHAMOMILLA WHOLE;
  • 12 [hp_X]/mL NITRIC ACID;
  • 12 [hp_X]/mL ORNITHOGALUM UMBELLATUM WHOLE;
  • 12 [hp_X]/mL PASSIFLORA INCARNATA FLOWERING TOP;
  • 12 [hp_X]/mL PHOSPHORUS;
  • 12 [hp_X]/mL PRUNUS CERASIFERA FLOWER;
  • 12 [hp_X]/mL SEPIA OFFICINALIS JUICE;
  • 12 [hp_X]/mL SILICON DIOXIDE;
  • 12 [hp_X]/mL SILVER NITRATE;
  • 12 [hp_X]/mL SODIUM CHLORIDE;
  • 12 [hp_X]/mL STRYCHNOS IGNATII SEED;
  • 12 [hp_X]/mL SULFUR;
  • 6 [hp_X]/mL SUS SCROFA HYPOTHALAMUS;
  • 6 [hp_X]/mL SUS SCROFA PITUITARY GLAND;
  • 12 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF;
  • 12 [hp_X]/mL VERATRUM ALBUM ROOT


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Bee Venoms [CS];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Standardized Insect Venom Allergenic Extract [EPC]

Labeler Information

Labeler Name: Body Wisdom Center for Healing
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/11/2020

Package Information

No. Package Code Package Description Billing Unit
173448-0001-130 mL in 1 BOTTLE, SPRAY (73448-0001-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73448-0001The 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 NAMERecalibr8The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEHypophysis Suis, Hypothalamus Suis, Aconitum Napellus, Aloe, Alumina, Antimonium Crudum, Apis Mellifica, Argentum Nitricum, Arnica Montana, Arsenicum Album, Belladonna, Bellis Perennis, Bryonia (Alba), Calcarea Fluorica, Calendula Officinalis, Causticum, Chamomilla, Chelidonium Majus, Cistus Canadensis, Clematis Erecta, Ferrum Phosphoricum, Gambogia, Graphites, Histaminum Hydrochloricum, Hydrastis canadensis, Hydrofluoricum Acidum, Hypericum Perforatum, Ignatia amara, Impatiens Glandulifera, Flos,The 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 DATE3/11/2020This 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 NAMEBody Wisdom Center for HealingName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACONITUM NAPELLUS WHOLE; ALLYLTHIOUREA; ALOE; ALUMINUM OXIDE; ANTIMONY TRISULFIDE; APIS MELLIFERA; ARNICA MONTANA WHOLE; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BELLIS PERENNIS WHOLE; BRYONIA ALBA ROOT; CALCIUM FLUORIDE; CALENDULA OFFICINALIS FLOWERING TOP; CAUSTICUM; CHELIDONIUM MAJUS WHOLE; CLEMATIS RECTA FLOWERING TOP; COMFREY ROOT; FERROSOFERRIC PHOSPHATE; GAMBOGE; GOLDENSEAL; GRAPHITE; HELIANTHEMUM CANADENSE; HISTAMINE DIHYDROCHLORIDE; HYDROFLUORIC ACID; HYPERICUM PERFORATUM WHOLE; IMPATIENS GLANDULIFERA FLOWER; LACHESIS MUTA VENOM; LEAD; LYCOPODIUM CLAVATUM SPORE; MATRICARIA CHAMOMILLA WHOLE; NITRIC ACID; ORNITHOGALUM UMBELLATUM WHOLE; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORUS; PRUNUS CERASIFERA FLOWER; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SILVER NITRATE; SODIUM CHLORIDE; STRYCHNOS IGNATII SEED; SULFUR; SUS SCROFA HYPOTHALAMUS; SUS SCROFA PITUITARY GLAND; TOXICODENDRON PUBESCENS LEAF; VERATRUM ALBUM ROOTAn 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 STRENGTH12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 6; 6; 12; 12 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC] 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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