Recalibr8

Product NDC
73448-0001
11-digit product format
734480001
Labeler code
73448
Product ID
73448-0001_6ef3de46-cb81-4bb0-91f4-f96586f2b309
Type
HUMAN OTC DRUG
Nonproprietary 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,
Dosage form
LIQUID
Route
ORAL
Labeler
Body Wisdom Center for Healing
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-03-11
Marketing end
0000-00-00
Substance
SUS SCROFA PITUITARY GLAND; SUS SCROFA HYPOTHALAMUS; ACONITUM NAPELLUS WHOLE; ALOE; ALUMINUM OXIDE; ANTIMONY TRISULFIDE; APIS MELLIFERA; SILVER NITRATE; ARNICA MONTANA WHOLE; ARSENIC TRIOXIDE; ATROPA BELLADONNA; BELLIS PERENNIS WHOLE; BRYONIA ALBA ROOT; CALCIUM FLUORIDE; CALENDULA OFFICINALIS FLOWERING TOP; CAUSTICUM; MATRICARIA CHAMOMILLA WHOLE; CHELIDONIUM MAJUS WHOLE; HELIANTHEMUM CANADENSE; CLEMATIS RECTA FLOWERING TOP; FERROSOFERRIC PHOSPHATE; GAMBOGE; GRAPHITE; HISTAMINE DIHYDROCHLORIDE; GOLDENSEAL; HYDROFLUORIC ACID; HYPERICUM PERFORATUM WHOLE; STRYCHNOS IGNATII SEED; IMPATIENS GLANDULIFERA FLOWER; LACHESIS MUTA VENOM; LYCOPODIUM CLAVATUM SPORE; SODIUM CHLORIDE; NITRIC ACID; ORNITHOGALUM UMBELLATUM WHOLE; PASSIFLORA INCARNATA FLOWERING TOP; PHOSPHORUS; LEAD; PRUNUS CERASIFERA FLOWER; TOXICODENDRON PUBESCENS LEAF; SEPIA OFFICINALIS JUICE; SILICON DIOXIDE; SULFUR; COMFREY ROOT; ALLYLTHIOUREA; VERATRUM ALBUM ROOT
Active strength
6 [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
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73448-0001-17344800010130 mL in 1 BOTTLE, SPRAY (73448-0001-1) 30 ml2020-03-110000-00-00NoNoCurrent