44911-0649 NDC - MULTI-PHENOLIC (MANNOSE, 5-HYDROXYTRYPTOPHAN, ACETALDEHYDE, ACETYLCHOLINE CHLORIDE, ASCORBICUM ACIDUM, ASPARTAME, BUTYLATED HYDROXYTOLUENE, CAFFEIC ACID, CANDIDA ALBICANS, CINNAMIC ACID, CONIFERYL ALCOHOL, COUMARINUM, DOPAMINE HYDROCHLORIDE, ESTRADIOL, GABA (GAMMA-AMINOBUTYRIC ACID), GALLICUM ACIDUM, HISTAMINUM HYDROCHLORICUM, HYDROCORTISONE, INDOLUM, L-DOPA, L-PHENYLALANINE, MELATONIN, MENADIONE, NOREPINEPHRINE (BITARTRATE), PETROSELINUM CRISPUM, PHENYL ISOTHIOCYANATE, PIPERINE, PROGESTERONE, PYRROLE, QUERCETIN,)

Drug Information

  • Product NDC: 44911-0649
  • Proprietary Name: Multi-Phenolic
  • Non Proprietary Name: Mannose, 5-Hydroxytryptophan, Acetaldehyde, Acetylcholine Chloride, Ascorbicum Acidum, Aspartame, Butylated Hydroxytoluene, Caffeic Acid, Candida Albicans, Cinnamic Acid, Coniferyl Alcohol, Coumarinum, Dopamine Hydrochloride, Estradiol, Gaba (Gamma-Aminobutyric Acid), Gallicum Acidum, Histaminum Hydrochloricum, Hydrocortisone, Indolum, L-Dopa, L-Phenylalanine, Melatonin, Menadione, Norepinephrine (Bitartrate), Petroselinum Crispum, Phenyl Isothiocyanate, Piperine, Progesterone, Pyrrole, Quercetin,
  • Active Ingredient(s): 12 [hp_X]/mL .GAMMA.-AMINOBUTYRIC ACID; 12 [hp_X]/mL ACETALDEHYDE; 12 [hp_X]/mL ACETYLCHOLINE CHLORIDE; 12 [hp_X]/mL ASCORBIC ACID; 12 [hp_X]/mL ASPARTAME; 12 [hp_X]/mL BUTYLATED HYDROXYTOLUENE; 12 [hp_X]/mL CAFFEIC ACID; 12 [hp_X]/mL CANDIDA ALBICANS; 16 [hp_X]/mL CHLOROGENIC ACID; 12 [hp_X]/mL CINNAMIC ACID; 12 [hp_X]/mL CONIFERYL ALCOHOL; 12 [hp_X]/mL COUMARIN; 12 [hp_X]/mL DOPAMINE HYDROCHLORIDE; 12 [hp_X]/mL ESTRADIOL; 12 [hp_X]/mL GALLIC ACID MONOHYDRATE; 12 [hp_X]/mL HISTAMINE DIHYDROCHLORIDE; 12 [hp_X]/mL HYDROCORTISONE; 12 [hp_X]/mL INDOLE; 12 [hp_X]/mL LEVODOPA; 12 [hp_C]/mL MALVIN; 12 [hp_X]/mL MANNOSE, D-; 12 [hp_X]/mL MELATONIN; 12 [hp_X]/mL MENADIONE; 12 [hp_X]/mL NOREPINEPHRINE BITARTRATE; 12 [hp_X]/mL OXITRIPTAN; 12 [hp_X]/mL PETROSELINUM CRISPUM WHOLE; 12 [hp_X]/mL PHENYL ISOTHIOCYANATE; 12 [hp_X]/mL PHENYLALANINE; 16 [hp_X]/mL PHLORIZIN; 12 [hp_X]/mL PIPERINE; 12 [hp_X]/mL PROGESTERONE; 12 [hp_X]/mL PYRROLE; 12 [hp_X]/mL QUERCETIN; 12 [hp_X]/mL RUTIN; 12 [hp_X]/mL SEROTONIN HYDROCHLORIDE; 12 [hp_X]/mL TAURINE; 12 [hp_X]/mL TYRAMINE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Amino Acids; Aromatic [CS]; Aromatic Amino Acid [EPC]; Ascorbic Acid [CS]; Catecholamine [EPC]; Catecholamine [EPC]; Catecholamines [CS]; Catecholamines [CS]; Cell-mediated Immunity [PE]; Cholinergic Agonists [MoA]; Cholinergic Receptor Agonist [EPC]; Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]; Estradiol Congeners [CS]; Estrogen Receptor Agonists [MoA]; Estrogen [EPC]; Fungal Proteins [CS]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Fungal Allergenic Extract [EPC]; Progesterone [CS]; Progesterone [EPC]; Vitamin C [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Energique, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/11/2022

Package Information

No. Package Code Package Description Billing Unit
144911-0649-130 mL in 1 BOTTLE, DROPPER (44911-0649-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0649The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMEMulti-PhenolicThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEMannose, 5-Hydroxytryptophan, Acetaldehyde, Acetylcholine Chloride, Ascorbicum Acidum, Aspartame, Butylated Hydroxytoluene, Caffeic Acid, Candida Albicans, Cinnamic Acid, Coniferyl Alcohol, Coumarinum, Dopamine Hydrochloride, Estradiol, Gaba (Gamma-Aminobutyric Acid), Gallicum Acidum, Histaminum Hydrochloricum, Hydrocortisone, Indolum, L-Dopa, L-Phenylalanine, Melatonin, Menadione, Norepinephrine (Bitartrate), Petroselinum Crispum, Phenyl Isothiocyanate, Piperine, Progesterone, Pyrrole, Quercetin,The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/11/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEEnergique, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME.GAMMA.-AMINOBUTYRIC ACID; ACETALDEHYDE; ACETYLCHOLINE CHLORIDE; ASCORBIC ACID; ASPARTAME; BUTYLATED HYDROXYTOLUENE; CAFFEIC ACID; CANDIDA ALBICANS; CHLOROGENIC ACID; CINNAMIC ACID; CONIFERYL ALCOHOL; COUMARIN; DOPAMINE HYDROCHLORIDE; ESTRADIOL; GALLIC ACID MONOHYDRATE; HISTAMINE DIHYDROCHLORIDE; HYDROCORTISONE; INDOLE; LEVODOPA; MALVIN; MANNOSE, D-; MELATONIN; MENADIONE; NOREPINEPHRINE BITARTRATE; OXITRIPTAN; PETROSELINUM CRISPUM WHOLE; PHENYL ISOTHIOCYANATE; PHENYLALANINE; PHLORIZIN; PIPERINE; PROGESTERONE; PYRROLE; QUERCETIN; RUTIN; SEROTONIN HYDROCHLORIDE; TAURINE; TYRAMINEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 12; 12; 12; 12; 12; 16; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 16; 12; 12; 12; 12; 12; 12; 12; 12 
ACTIVE INGRED UNIT[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_C]/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 
PHARM CLASSESAllergens [CS], Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC], Ascorbic Acid [CS], Catecholamine [EPC], Catecholamine [EPC], Catecholamines [CS], Catecholamines [CS], Cell-mediated Immunity [PE], Cholinergic Agonists [MoA], Cholinergic Receptor Agonist [EPC], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC], Progesterone [CS], Progesterone [EPC], Vitamin C [EPC] 

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This page was last updated on: 4/4/2025

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