Regional Allergies Desert U.S.

Product NDC
57955-2806
11-digit product format
579552806
Labeler code
57955
Product ID
57955-2806_10f2b00e-dea8-4006-94bd-3097730ebfd4
Type
HUMAN OTC DRUG
Nonproprietary name
Adenosinum cyclophosphoricum, Adrenalinum, Adrenalinum, Adrenalinum, Allium cepa, Ambrosia artemisiaefolia, Arum triphyllum, Arundo mauritanica, Cortisone aceticum, Erechtites hieracifolia, Erigeron canadensis, Euonymus atropurpureus, Euphrasia officinalis, Galphimia glauca,Histaminum hydrochloricum, Kali muriaticum, Natrum muriaticum, RNA, Sabadilla, Stramonium, Triticum repens
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-04-18
Marketing end
0000-00-00
Substance
ADENOSINE CYCLIC PHOSPHATE; AMBROSIA ARTEMISIIFOLIA WHOLE; ARISAEMA TRIPHYLLUM ROOT; ARUNDO PLINIANA ROOT; CORTICOTROPIN; CORTISONE ACETATE; DATURA STRAMONIUM; ELYMUS REPENS ROOT; EPINEPHRINE; ERECHTITES HIERACIIFOLIUS WHOLE; ERIGERON CANADENSIS WHOLE; EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; MEDICAGO SATIVA WHOLE; ONION; POTASSIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; SCHOENOCAULON OFFICINALE SEED; SODIUM CHLORIDE
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
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 formatDescriptionMarketing startMarketing endSampleExclude flagStatus
57955-2806-2579552806021 BOTTLE, SPRAY in 1 CARTON (57955-2806-2) > 59 mL in 1 BOTTLE, SPRAY2022-04-180000-00-00NoNoCurrent