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 NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 57955-2806-2 | 57955280602 | 1 BOTTLE, SPRAY in 1 CARTON (57955-2806-2) > 59 mL in 1 BOTTLE, SPRAY | 2022-04-18 | 0000-00-00 | No | No | Current |