64578-0148 NDC - ALLER-CHORD F (ACETALDEHYDE, ACETICUM AC, ARG NIT, CAFFEINUM, CALC SULPH, CITRICUM AC, CORTISONE ACETICUM, ECHINACEA PURP, FOLLICULINUM, FRAGARIA, FUMARICUM AC, GALLICUM AC, GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, HISTAMINUM HYDROCHLORICUM, HYDRANGEA, LAC VAC, LECITHIN, LIMULUS, LYCOPERSICUM, LYCOPODIUM, NAT BICARB, NAT MUR, NUX VOM, PARAFFINUM, PHOSPHORICUM AC, SACCHARUM OFF, SILICEA, TARTARICUM AC, TORULA CEREVISIAE.)

Drug Information

  • Product NDC: 64578-0148
  • Proprietary Name: Aller-Chord F
  • Non Proprietary Name: Acetaldehyde, Aceticum ac, Arg nit, Caffeinum, Calc sulph, Citricum ac, Cortisone aceticum, Echinacea purp, Folliculinum, Fragaria, Fumaricum ac, Gallicum ac, Glandula suprarenalis suis, Hepar suis, Histaminum hydrochloricum, Hydrangea, Lac vac, Lecithin, Limulus, Lycopersicum, Lycopodium, Nat bicarb, Nat mur, Nux vom, Paraffinum, Phosphoricum ac, Saccharum off, Silicea, Tartaricum ac, Torula cerevisiae.
  • Active Ingredient(s): 12 [hp_X]/59.1mL ACETALDEHYDE; 15 [hp_X]/59.1mL ACETIC ACID; 15 [hp_X]/59.1mL ALPINE STRAWBERRY; 15 [hp_X]/59.1mL ANHYDROUS CITRIC ACID; 15 [hp_X]/59.1mL CAFFEINE; 15 [hp_X]/59.1mL CALCIUM SULFATE ANHYDROUS; 20 [hp_X]/59.1mL CORTISONE ACETATE; 15 [hp_X]/59.1mL COW MILK; 6 [hp_X]/59.1mL ECHINACEA PURPUREA; 15 [hp_X]/59.1mL EGG PHOSPHOLIPIDS; 15 [hp_X]/59.1mL ESTRONE; 15 [hp_X]/59.1mL FUMARIC ACID; 12 [hp_X]/59.1mL GALLIC ACID MONOHYDRATE; 12 [hp_X]/59.1mL HISTAMINE DIHYDROCHLORIDE; 6 [hp_X]/59.1mL HYDRANGEA ARBORESCENS ROOT; 15 [hp_X]/59.1mL LIMULUS POLYPHEMUS; 12 [hp_X]/59.1mL LYCOPODIUM CLAVATUM SPORE; 15 [hp_X]/59.1mL PARAFFIN; 15 [hp_X]/59.1mL PHOSPHORIC ACID; 9 [hp_X]/59.1mL PORK LIVER; 15 [hp_X]/59.1mL SACCHAROMYCES CEREVISIAE; 15 [hp_X]/59.1mL SILICON DIOXIDE; 10 [hp_X]/59.1mL SILVER NITRATE; 15 [hp_X]/59.1mL SODIUM BICARBONATE; 12 [hp_X]/59.1mL SODIUM CHLORIDE; 15 [hp_X]/59.1mL SOLANUM LYCOPERSICUM; 12 [hp_X]/59.1mL STRYCHNOS NUX-VOMICA SEED; 15 [hp_X]/59.1mL SUCROSE; 9 [hp_X]/59.1mL SUS SCROFA ADRENAL GLAND; 15 [hp_X]/59.1mL TARTARIC ACID
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Acidifying Activity [MoA]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Anti-coagulant [EPC]; Blood Coagulation Factor [EPC]; Calcium Chelating Activity [MoA]; Calcium [CS]; Calculi Dissolution Agent [EPC]; Cations; Divalent [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Central Nervous System Stimulant [EPC]; Central Nervous System Stimulation [PE]; Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]; Decreased Coagulation Factor Activity [PE]; Dietary Proteins [CS]; Dietary Proteins [CS]; Fungal Proteins [CS]; Fungal Proteins [CS]; Increased Coagulation Factor Activity [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Increased IgG Production [PE]; Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Methylxanthine [EPC]; Milk Proteins [CS]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Fungal Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Plant Proteins [CS]; Seed Storage Proteins [CS]; Xanthines [CS]

Labeler Information

Field Name Field Value
Labeler Name: Energetix Corp
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:8/8/2014

Package Information

No. Package Code Package Description Billing Unit
164578-0148-159.1 mL in 1 BOTTLE, DROPPER (64578-0148-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0148The 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 NAMEAller-Chord FThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAcetaldehyde, Aceticum ac, Arg nit, Caffeinum, Calc sulph, Citricum ac, Cortisone aceticum, Echinacea purp, Folliculinum, Fragaria, Fumaricum ac, Gallicum ac, Glandula suprarenalis suis, Hepar suis, Histaminum hydrochloricum, Hydrangea, Lac vac, Lecithin, Limulus, Lycopersicum, Lycopodium, Nat bicarb, Nat mur, Nux vom, Paraffinum, Phosphoricum ac, Saccharum off, Silicea, Tartaricum ac, Torula cerevisiae.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 DATE8/8/2014This 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 NAMEEnergetix CorpName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACETALDEHYDE; ACETIC ACID; ALPINE STRAWBERRY; ANHYDROUS CITRIC ACID; CAFFEINE; CALCIUM SULFATE ANHYDROUS; CORTISONE ACETATE; COW MILK; ECHINACEA PURPUREA; EGG PHOSPHOLIPIDS; ESTRONE; FUMARIC ACID; GALLIC ACID MONOHYDRATE; HISTAMINE DIHYDROCHLORIDE; HYDRANGEA ARBORESCENS ROOT; LIMULUS POLYPHEMUS; LYCOPODIUM CLAVATUM SPORE; PARAFFIN; PHOSPHORIC ACID; PORK LIVER; SACCHAROMYCES CEREVISIAE; SILICON DIOXIDE; SILVER NITRATE; SODIUM BICARBONATE; SODIUM CHLORIDE; SOLANUM LYCOPERSICUM; STRYCHNOS NUX-VOMICA SEED; SUCROSE; SUS SCROFA ADRENAL GLAND; TARTARIC ACIDAn 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; 15; 15; 15; 15; 15; 20; 15; 6; 15; 15; 15; 12; 12; 6; 15; 12; 15; 15; 9; 15; 15; 10; 15; 12; 15; 12; 15; 9; 15 
ACTIVE INGRED UNIT[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL 
PHARM CLASSESAcidifying Activity [MoA], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Anti-coagulant [EPC], Blood Coagulation Factor [EPC], Calcium Chelating Activity [MoA], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Decreased Coagulation Factor Activity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Fungal Proteins [CS], Fungal Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Methylxanthine [EPC], Milk Proteins [CS], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Fungal Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Seed Storage Proteins [CS], Xanthines [CS] 

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This page was last updated on: 7/4/2025

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