63479-0612 NDC - F12 (ALOE VERA, AVOCADO, BERBERIS AQUIFOLIUM, CALOCHORTUS TOLMIE, CAROBA, CHAMOMILE, CORNSILK, DILL, FAGUS SYLVATICA, GOLD, HYPERICUM PERFORATUM, ILEX AQUIFOLIUM, JUGLANS REGIA, LAVENDER, LYCOPODIUM CLAVATUM, MADIA ELEGANS, MEADIA HENDERSONII, MONARDELLA, MORNING GLORY, NAJA TRIPUDIANS, PENSTEMON DAVIDSONII, PHOSPHORUS, PRUNUS PERSICA, PSORINUM, PULSATILLA VULGARIS, RED CLOVER, ROSA CALIFORNICA, SACRED LOTUS, SARSAPARILLA, SILENE LACINIATA, SILVER, SOLIDAGO CALIFORNICA, SPIDERWORT, WHITE WILLOW)

Drug Information

Product NDC: 63479-0612

Proprietary Name: F12

Non Proprietary Name: ALOE VERA, AVOCADO, BERBERIS AQUIFOLIUM, CALOCHORTUS TOLMIE, CAROBA, CHAMOMILE, CORNSILK, DILL, FAGUS SYLVATICA, GOLD, HYPERICUM PERFORATUM, ILEX AQUIFOLIUM, JUGLANS REGIA, LAVENDER, LYCOPODIUM CLAVATUM, MADIA ELEGANS, MEADIA HENDERSONII, MONARDELLA, MORNING GLORY, NAJA TRIPUDIANS, PENSTEMON DAVIDSONII, PHOSPHORUS, PRUNUS PERSICA, PSORINUM, PULSATILLA VULGARIS, RED CLOVER, ROSA CALIFORNICA, SACRED LOTUS, SARSAPARILLA, SILENE LACINIATA, SILVER, SOLIDAGO CALIFORNICA, SPIDERWORT, WHITE WILLOW

Active Ingredient(s):
  • 12 [hp_C]/mL ALOE VERA FLOWER;
  • 12 [hp_C]/mL ANETHUM GRAVEOLENS WHOLE;
  • 12 [hp_C]/mL BERBERIS AQUIFOLIUM WHOLE;
  • 12 [hp_C]/mL CALOCHORTUS TOLMIEI WHOLE;
  • 12 [hp_C]/mL CHAMOMILE;
  • 12 [hp_C]/mL CORN SILK;
  • 12 [hp_C]/mL FAGUS SYLVATICA FLOWERING TOP;
  • 12 [hp_C]/mL GOLD;
  • 12 [hp_C]/mL HYPERICUM PERFORATUM FLOWER;
  • 12 [hp_C]/mL ILEX AQUIFOLIUM FLOWERING TOP;
  • 12 [hp_C]/mL IPOMOEA PURPUREA TOP;
  • 12 [hp_C]/mL JACARANDA CAROBA FLOWER;
  • 12 [hp_C]/mL JUGLANS REGIA FLOWERING TOP;
  • 12 [hp_C]/mL LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER;
  • 12 [hp_C]/mL LYCOPODIUM CLAVATUM SPORE;
  • 12 [hp_C]/mL MADIA ELEGANS WHOLE;
  • 12 [hp_C]/mL MONARDELLA ODORATISSIMA WHOLE;
  • 12 [hp_C]/mL NAJA NAJA VENOM;
  • 12 [hp_C]/mL NELUMBO NUCIFERA FLOWER;
  • 12 [hp_C]/mL PENSTEMON DAVIDSONII WHOLE;
  • 12 [hp_C]/mL PERSEA AMERICANA WHOLE;
  • 15 [hp_C]/mL PHOSPHORUS;
  • 12 [hp_C]/mL PRIMULA HENDERSONII WHOLE;
  • 12 [hp_C]/mL PRUNUS PERSICA VAR. NUCIPERSICA WHOLE;
  • 15 [hp_C]/mL PULSATILLA VULGARIS WHOLE;
  • 12 [hp_C]/mL ROSA CALIFORNICA WHOLE;
  • 12 [hp_C]/mL SALIX ALBA FLOWERING TOP;
  • 15 [hp_C]/mL SARSAPARILLA;
  • 12 [hp_C]/mL SCABIES LESION LYSATE (HUMAN);
  • 12 [hp_C]/mL SILENE LACINIATA WHOLE;
  • 12 [hp_C]/mL SILVER;
  • 12 [hp_C]/mL SOLIDAGO CALIFORNICA WHOLE;
  • 12 [hp_C]/mL TRADESCANTIA OCCIDENTALIS WHOLE;
  • 12 [hp_C]/mL TRIFOLIUM PRATENSE FLOWER


Administration Route(s): SUBLINGUAL

Dosage Form(s): SOLUTION/ DROPS

Pharmacy Class(es):
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Increased Histamine Release [PE];
  • Standardized Chemical Allergen [EPC]

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
163479-0612-130 mL in 1 BOTTLE, GLASS (63479-0612-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC63479-0612The 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 NAMEF12The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIXPSTVTYA 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 NAMEALOE VERA, AVOCADO, BERBERIS AQUIFOLIUM, CALOCHORTUS TOLMIE, CAROBA, CHAMOMILE, CORNSILK, DILL, FAGUS SYLVATICA, GOLD, HYPERICUM PERFORATUM, ILEX AQUIFOLIUM, JUGLANS REGIA, LAVENDER, LYCOPODIUM CLAVATUM, MADIA ELEGANS, MEADIA HENDERSONII, MONARDELLA, MORNING GLORY, NAJA TRIPUDIANS, PENSTEMON DAVIDSONII, PHOSPHORUS, PRUNUS PERSICA, PSORINUM, PULSATILLA VULGARIS, RED CLOVER, ROSA CALIFORNICA, SACRED LOTUS, SARSAPARILLA, SILENE LACINIATA, SILVER, SOLIDAGO CALIFORNICA, SPIDERWORT, WHITE WILLOWThe 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 NAMEALOE VERA FLOWER; ANETHUM GRAVEOLENS WHOLE; BERBERIS AQUIFOLIUM WHOLE; CALOCHORTUS TOLMIEI WHOLE; CHAMOMILE; CORN SILK; FAGUS SYLVATICA FLOWERING TOP; GOLD; HYPERICUM PERFORATUM FLOWER; ILEX AQUIFOLIUM FLOWERING TOP; IPOMOEA PURPUREA TOP; JACARANDA CAROBA FLOWER; JUGLANS REGIA FLOWERING TOP; LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER; LYCOPODIUM CLAVATUM SPORE; MADIA ELEGANS WHOLE; MONARDELLA ODORATISSIMA WHOLE; NAJA NAJA VENOM; NELUMBO NUCIFERA FLOWER; PENSTEMON DAVIDSONII WHOLE; PERSEA AMERICANA WHOLE; PHOSPHORUS; PRIMULA HENDERSONII WHOLE; PRUNUS PERSICA VAR. NUCIPERSICA WHOLE; PULSATILLA VULGARIS WHOLE; ROSA CALIFORNICA WHOLE; SALIX ALBA FLOWERING TOP; SARSAPARILLA; SCABIES LESION LYSATE (HUMAN); SILENE LACINIATA WHOLE; SILVER; SOLIDAGO CALIFORNICA WHOLE; TRADESCANTIA OCCIDENTALIS WHOLE; TRIFOLIUM PRATENSE FLOWERAn 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; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 12; 15; 12; 12; 15; 12; 12; 15; 12; 12; 12; 12; 12; 12 
ACTIVE INGRED UNIT[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_C]/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_C]/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_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL; [hp_C]/mL 
PHARM CLASSESAllergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC] 

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This page was last updated on: 2/1/2023