Regional Allergies Rocky Mtns. U.S.

Product NDC
57955-0756
11-digit product format
579550756
Labeler code
57955
Product ID
57955-0756_cb9296ae-b4eb-4a0c-bc99-c45dcf9c0e38
Type
HUMAN OTC DRUG
Nonproprietary name
Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Agrimonia eupatoria, Agrostemma githago, Ailanthus glandulosus, Allium cepa, Arum triphyllum, Arundo mauritanica, Cortisone aceticum, Cynodon dactylon, Equisetum hyemale, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Kali muriaticum, Natrum muriaticum, Platanus, Populus candicans, RNA, Sabadilla, Solidago virgaurea.
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-07-13
Marketing end
0000-00-00
Substance
ADENOSINE CYCLIC PHOSPHATE; AGRIMONIA EUPATORIA WHOLE; AGROSTEMMA GITHAGO SEED; AILANTHUS ALTISSIMA FLOWERING TWIG; ARISAEMA TRIPHYLLUM ROOT; ARUNDO PLINIANA ROOT; CORTICOTROPIN; CORTISONE ACETATE; CYNODON DACTYLON WHOLE; EPINEPHRINE; EQUISETUM HYEMALE WHOLE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; ONION; PLATANUS OCCIDENTALIS WHOLE; POPULUS BALSAMIFERA LEAF BUD; POTASSIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; SCHOENOCAULON OFFICINALE SEED; SODIUM CHLORIDE; SOLIDAGO VIRGAUREA FLOWERING TOP
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 formatDescriptionMarketing startMarketing endSampleExclude flagStatus
57955-0756-2579550756021 BOTTLE, SPRAY in 1 CARTON (57955-0756-2) > 59 mL in 1 BOTTLE, SPRAY2022-07-130000-00-00NoNoCurrent