Allergies Southern U.S.

Product NDC
57955-3721
11-digit product format
579553721
Labeler code
57955
Product ID
57955-3721_59ece124-d644-41a0-bec6-0f748ae6fc69
Type
HUMAN OTC DRUG
Nonproprietary name
Adenosinum cycloposphorcum, Adrenalinum, Adrenocorticotrophin, Allium cepa, Alnus ser, Arum triph, Arundo, Carduus ben, Cichorium int, Cortisone aceticum, Dolichos, Euphrasia, Galphimia, Histaminum hydrochloricum, Juglans cin, Kali mur, Nasturtium, Nat mur, Rhus tox RNA, Sabaadilla, Sassafras.
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-04-27
Marketing end
0000-00-00
Substance
ADENOSINE CYCLIC PHOSPHATE; ALNUS SERRULATA BARK; ARISAEMA TRIPHYLLUM ROOT; ARUNDO PLINIANA ROOT; CENTAUREA BENEDICTA; CHICORY ROOT; CORTICOTROPIN; CORTISONE ACETATE; EPINEPHRINE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; JUGLANS CINEREA BRANCH BARK/ROOT BARK; MUCUNA PRURIENS FRUIT TRICHOME; NASTURTIUM OFFICINALE; ONION; POTASSIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; SASSAFRAS ALBIDUM ROOT BARK; SCHOENOCAULON OFFICINALE SEED; SODIUM CHLORIDE; TOXICODENDRON PUBESCENS LEAF
Active strength
12 [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL
Pharmacologic classes
Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Vegetable Proteins [CS], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57955-3721-25795537210259 mL in 1 BOTTLE, SPRAY (57955-3721-2) 59 ml2022-04-270000-00-00NoNoCurrent