63479-0618 NDC - F18 (APRICOT, CHAMOMILE, COFFEA ARABICA, COFFEA CRUDA, COMFREY, CRIMSON MONKEY, DATE PALM, DILL, ENGLISH ELM ING TWIG, EUROPEAN ASPEN, FILAREE, GOLDEN EARDROPS, HORSE CHESTNUT, HUMULUS LUPULUS, HYPERICUM PERFORATUM, HYPERICUM PERFORATUM FLOWER, IMPATIENS GLANDULIFERA, MAGNESIA PHOSPHORICA, MEXICAN PINK, MIMULUS GUTTATUS, NUX VOMICA, OREGON GRAPEHOLLY, PASSIFLORA INCARNATA, SCUTELLARIA LATERIFLORA, SWEET CHESTNUT, VERBENA OFFICINALIS, WATERMELON, YERBA SANTA, ZINCUM VALERIANICUM)

Drug Information

Product NDC: 63479-0618

Proprietary Name: F18

Non Proprietary Name: APRICOT, CHAMOMILE, COFFEA ARABICA, COFFEA CRUDA, COMFREY, CRIMSON MONKEY, DATE PALM, DILL, ENGLISH ELM ING TWIG, EUROPEAN ASPEN, FILAREE, GOLDEN EARDROPS, HORSE CHESTNUT, HUMULUS LUPULUS, HYPERICUM PERFORATUM, HYPERICUM PERFORATUM FLOWER, IMPATIENS GLANDULIFERA, MAGNESIA PHOSPHORICA, MEXICAN PINK, MIMULUS GUTTATUS, NUX VOMICA, OREGON GRAPEHOLLY, PASSIFLORA INCARNATA, SCUTELLARIA LATERIFLORA, SWEET CHESTNUT, VERBENA OFFICINALIS, WATERMELON, YERBA SANTA, ZINCUM VALERIANICUM

Active Ingredient(s):
  • 12 [hp_C]/mL AESCULUS HIPPOCASTANUM FLOWER;
  • 12 [hp_C]/mL ANETHUM GRAVEOLENS WHOLE;
  • 15 [hp_X]/mL ARABICA COFFEE BEAN;
  • 12 [hp_C]/mL BERBERIS AQUIFOLIUM WHOLE;
  • 12 [hp_C]/mL CALOCHORTUS GUNNISONII WHOLE;
  • 12 [hp_C]/mL CASTANEA SATIVA FLOWER;
  • 12 [hp_C]/mL COFFEA ARABICA WHOLE;
  • 12 [hp_C]/mL EHRENDORFERIA CHRYSANTHA WHOLE;
  • 12 [hp_C]/mL ERIODICTYON CALIFORNICUM FLOWERING TOP;
  • 12 [hp_C]/mL ERODIUM CICUTARIUM;
  • 12 [hp_C]/mL ERYTHRANTHE CARDINALIS WHOLE;
  • 4 [hp_X]/mL HOPS;
  • 4 [hp_X]/mL HYPERICUM PERFORATUM;
  • 12 [hp_C]/mL HYPERICUM PERFORATUM FLOWER;
  • 12 [hp_C]/mL IMPATIENS GLANDULIFERA FLOWER;
  • 10 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE;
  • 12 [hp_C]/mL MATRICARIA RECUTITA FLOWERING TOP;
  • 12 [hp_C]/mL MIMULUS GUTTATUS FLOWERING TOP;
  • 4 [hp_X]/mL PASSIFLORA INCARNATA FLOWERING TOP;
  • 12 [hp_C]/mL PHOENIX DACTYLIFERA WHOLE;
  • 12 [hp_C]/mL POPULUS TREMULA FLOWERING TOP;
  • 12 [hp_C]/mL PRUNUS ARMENIACA WHOLE;
  • 6 [hp_X]/mL SCUTELLARIA LATERIFLORA WHOLE;
  • 12 [hp_C]/mL SILENE LACINIATA WHOLE;
  • 10 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED;
  • 12 [hp_C]/mL SYMPHYTUM OFFICINALE WHOLE;
  • 12 [hp_C]/mL ULMUS PROCERA FLOWERING TWIG;
  • 12 [hp_C]/mL VERBENA OFFICINALIS FLOWERING TOP;
  • 12 [hp_C]/mL WATERMELON;
  • 12 [hp_X]/mL ZINC VALERATE DIHYDRATE


Administration Route(s): SUBLINGUAL

Dosage Form(s): SOLUTION/ DROPS

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Calculi Dissolution Agent [EPC];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Dietary Proteins [CS];
  • Dietary Proteins [CS];
  • Food Additives [CS];
  • Fruit Proteins [EXT];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE];
  • Magnesium Ion Exchange Activity [MoA];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Plant Proteins [CS];
  • Plant Proteins [CS];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS];
  • Seed Storage Proteins [CS];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Labeler Name: Apex Energetics Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/12/1996

Package Information

No. Package Code Package Description Billing Unit
163479-0618-130 mL in 1 BOTTLE, GLASS (63479-0618-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63479-0618The 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 NAMEF18The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXRLXTNA suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAMEAPRICOT, CHAMOMILE, COFFEA ARABICA, COFFEA CRUDA, COMFREY, CRIMSON MONKEY, DATE PALM, DILL, ENGLISH ELM ING TWIG, EUROPEAN ASPEN, FILAREE, GOLDEN EARDROPS, HORSE CHESTNUT, HUMULUS LUPULUS, HYPERICUM PERFORATUM, HYPERICUM PERFORATUM FLOWER, IMPATIENS GLANDULIFERA, MAGNESIA PHOSPHORICA, MEXICAN PINK, MIMULUS GUTTATUS, NUX VOMICA, OREGON GRAPEHOLLY, PASSIFLORA INCARNATA, SCUTELLARIA LATERIFLORA, SWEET CHESTNUT, VERBENA OFFICINALIS, WATERMELON, YERBA SANTA, ZINCUM VALERIANICUMThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMESOLUTION/ DROPSThe translation of the dosage form Code submitted by the firm.
ROUTE NAMESUBLINGUALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE3/12/1996This 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 NAMEApex Energetics Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEAESCULUS HIPPOCASTANUM FLOWER; ANETHUM GRAVEOLENS WHOLE; ARABICA COFFEE BEAN; BERBERIS AQUIFOLIUM WHOLE; CALOCHORTUS GUNNISONII WHOLE; CASTANEA SATIVA FLOWER; COFFEA ARABICA WHOLE; EHRENDORFERIA CHRYSANTHA WHOLE; ERIODICTYON CALIFORNICUM FLOWERING TOP; ERODIUM CICUTARIUM; ERYTHRANTHE CARDINALIS WHOLE; HOPS; HYPERICUM PERFORATUM; HYPERICUM PERFORATUM FLOWER; IMPATIENS GLANDULIFERA FLOWER; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MATRICARIA RECUTITA FLOWERING TOP; MIMULUS GUTTATUS FLOWERING TOP; PASSIFLORA INCARNATA FLOWERING TOP; PHOENIX DACTYLIFERA WHOLE; POPULUS TREMULA FLOWERING TOP; PRUNUS ARMENIACA WHOLE; SCUTELLARIA LATERIFLORA WHOLE; SILENE LACINIATA WHOLE; STRYCHNOS NUX-VOMICA SEED; SYMPHYTUM OFFICINALE WHOLE; ULMUS PROCERA FLOWERING TWIG; VERBENA OFFICINALIS FLOWERING TOP; WATERMELON; ZINC VALERATE DIHYDRATEAn 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; 15; 12; 12; 12; 12; 12; 12; 12; 12; 4; 4; 12; 12; 10; 12; 12; 4; 12; 12; 12; 6; 12; 10; 12; 12; 12; 12; 12 
ACTIVE INGRED UNIT[hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Dietary Proteins [CS], Food Additives [CS], Fruit Proteins [EXT], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Laxative [EPC], Plant Proteins [CS], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Seed Storage Proteins [CS], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] 

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