Allerphenex
- Product NDC
- 44911-0355
- 11-digit product format
- 449110355
- Labeler code
- 44911
- Product ID
- 44911-0355_9f8d1f0d-2729-48d0-bdd1-57d137d2893f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetylcholine Chloride, Acetaldehyde, Adrenalinum, Caffeic Acid, Candida Albicans, Chlorogenic Acid, Cinnamic Acid, Coumarinum, Cysteinum, Gallicum Acidum, Hepar Suis, Histaminum Hydrochloricum, Indolum, Malvin, Mannan, Menadione, Norepinephrine, Octopamine (Hydrochloride), Pancreas Suis, Phenyl Isothiocyanate, Phloridzinum, Quercetin, Salsolinol, Serotonin (Hydrochloride)
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2016-04-20
- Marketing end
- 2024-02-25
- Substance
- ACETALDEHYDE; ACETYLCHOLINE CHLORIDE; CAFFEIC ACID; CANDIDA ALBICANS; CHLOROGENIC ACID; CINNAMIC ACID; COUMARIN; CYSTEINE; EPINEPHRINE; GALLIC ACID MONOHYDRATE; HISTAMINE DIHYDROCHLORIDE; INDOLE; MALVIN; MENADIONE; NOREPINEPHRINE; OCTOPAMINE HYDROCHLORIDE; PHENYL ISOTHIOCYANATE; PHLORIZIN; PORK LIVER; QUERCETIN; SALSOLINOL HYDROCHLORIDE; SEROTONIN HYDROCHLORIDE; SUS SCROFA PANCREAS; YEAST MANNAN
- Active strength
- 200 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Allergens [CS], Catecholamine [EPC], Catecholamine [EPC], Catecholamines [CS], Catecholamines [CS], Cell-mediated Immunity [PE], Cholinergic Agonists [MoA], Cholinergic Receptor Agonist [EPC], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 44911-0355-1 | 44911035501 | 30 mL in 1 BOTTLE, DROPPER (44911-0355-1) | 30 ml | 2016-04-20 | 2024-02-25 | No | No | Current |