NDC 57955-2718

Allergies Desert U.S.

Adenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Alfalfa, Allium Cepa, Ambrosia, Cortisone Aceticum, Erechtites, Erigeron, Euonymus Atrop, Euphrasia, Galphimia, Histaminum Hydrochloricum, Kali Mur, Mucosa Nas, Nat Mur, Rna, Sabadilla, Stramonium, Triticum.

Allergies Desert U.S. is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by King Bio Inc.. The primary component is Adenosine Cyclic Phosphate; Epinephrine; Corticotropin; Alfalfa; Onion; Ambrosia Artemisiifolia; Cortisone Acetate; Erechtites Hieraciifolius; Conyza Canadensis; Euonymus Atropurpureus Branch Bark/root Bark; Euphrasia Stricta; Galphimia Glauca Flowering Top; Histamine Dihydrochloride; Potassium Chloride; Sus Scrofa Nasal Mucosa; Sodium Chloride; Saccharomyces Cerevisiae Rna; Schoenocaulon Officinale Seed; Datura Stramonium; Elymus Repens Root.

Product ID57955-2718_ca97beea-9303-4fad-bf5e-032641297611
NDC57955-2718
Product TypeHuman Otc Drug
Proprietary NameAllergies Desert U.S.
Generic NameAdenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Alfalfa, Allium Cepa, Ambrosia, Cortisone Aceticum, Erechtites, Erigeron, Euonymus Atrop, Euphrasia, Galphimia, Histaminum Hydrochloricum, Kali Mur, Mucosa Nas, Nat Mur, Rna, Sabadilla, Stramonium, Triticum.
Dosage FormLiquid
Route of AdministrationORAL
Marketing Start Date2018-05-25
Marketing CategoryUNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
Labeler NameKing Bio Inc.
Substance NameADENOSINE CYCLIC PHOSPHATE; EPINEPHRINE; CORTICOTROPIN; ALFALFA; ONION; AMBROSIA ARTEMISIIFOLIA; CORTISONE ACETATE; ERECHTITES HIERACIIFOLIUS; CONYZA CANADENSIS; EUONYMUS ATROPURPUREUS BRANCH BARK/ROOT BARK; EUPHRASIA STRICTA; GALPHIMIA GLAUCA FLOWERING TOP; HISTAMINE DIHYDROCHLORIDE; POTASSIUM CHLORIDE; SUS SCROFA NASAL MUCOSA; SODIUM CHLORIDE; SACCHAROMYCES CEREVISIAE RNA; SCHOENOCAULON OFFICINALE SEED; DATURA STRAMONIUM; ELYMUS REPENS ROOT
Active Ingredient Strength12 [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
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 57955-2718-2

59 mL in 1 BOTTLE, SPRAY (57955-2718-2)
Marketing Start Date2018-05-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 57955-2718-2 [57955271802]

Allergies Desert U.S. LIQUID
Marketing Categoryunapproved homeopathic
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-05-25
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ADENOSINE CYCLIC PHOSPHATE12 [hp_X]/59mL

OpenFDA Data

SPL SET ID:4c63ac20-f590-48a4-9754-67223a5a517c
Manufacturer
UNII

NDC Crossover Matching brand name "Allergies Desert U.S." or generic name "Adenosinum Cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Alfalfa, Allium Cepa, Ambrosia, Cortisone Aceticum, Erechtites, Erigeron, Euonymus Atrop, Euphrasia, Galphimia, Histaminum Hydrochloricum, Kali Mur, Mucosa Nas, Nat Mur, Rna, Sabadilla, Stramonium, Triticum."

NDCBrand NameGeneric Name
57955-2718Allergies Desert U.S.Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Alfalfa, Allium cepa, Ambrosia, Cortisone aceticum, Erechtites, Erigeron, Euonymus atrop, Euphrasia, Galphimia, Histaminum hydrochloricum, Kali mur, Mucosa nas, Nat mur, RNA, Sabadilla, Stramonium, Triticum.
57955-2722Allergies Desert U.S.Adenosinum cyclophosphoricum, Adrenalinum, Adrenocorticotrophin, Alfalfa, Allium cepa, Ambrosia, Arum triph, Arundo mauritanica, Cortisone aceticum, Erechtites, Erigeron, Euonymus atrop, Euphrasia, Galphimia, Nat mur, RNA, Sabadilla, Stramonium, Triticum

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