Allergies Northeast U.S.

Product NDC
57955-2712
11-digit product format
579552712
Labeler code
57955
Product ID
57955-2712_0bd017d0-2a2f-472b-b732-840d363fb604
Type
HUMAN OTC DRUG
Nonproprietary name
Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Agraphis, Allium cepa, Arum triph, Arundo mauritanica, Collinsonia, Cortisone aceticum, Euphrasia, Galphimia, Histaminum hydrochloricum, Kali mur, Nat mur, RNA, Rumex crisp, Sabadilla, Salvia, Tanacetum, Trifolium prat, Vinca
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-05-18
Marketing end
0000-00-00
Substance
ADENOSINE CYCLIC PHOSPHATE; ARISAEMA TRIPHYLLUM ROOT; ARUNDO PLINIANA ROOT; COLLINSONIA CANADENSIS ROOT; CORTICOTROPIN; CORTISONE ACETATE; EPINEPHRINE; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; HYACINTHOIDES NON-SCRIPTA WHOLE; ONION; PERVINCA MINOR WHOLE; POTASSIUM CHLORIDE; RUMEX CRISPUS ROOT; SACCHAROMYCES CEREVISIAE RNA; SAGE; SCHOENOCAULON OFFICINALE SEED; SODIUM CHLORIDE; TANACETUM VULGARE TOP; TRIFOLIUM PRATENSE FLOWER
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], Allergens [CS], Catecholamine [EPC], Catecholamines [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Dietary Proteins [CS], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], 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
57955-2712-25795527120259 mL in 1 BOTTLE, SPRAY (57955-2712-2) 59 ml2022-05-180000-00-00NoNoCurrent