B09 Solution/ Drops
NDC 63479-0209
View dosage, usage, ingredients, routes, and UNII mappings.
Product Information
B09 (aconitum napellus, arsenicum album, baptisia tinctoria, belladonna, bryonia, cherry plum, clematis vitalba, echinacea angustifolia, echinacea purpurea, eucalyptus globulus, eupatorium perfoliatum, european olive, ferrum phosphoricum, gentiana lutea, impatiens glandulifera, influenza a virus, lachesis mutus, luffa operculata, ornithogalum umbellatum, phosphorus, rockrose, sarcolacticum acidum, veratrum album, yellow jasmine) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Apex Energetics Inc.. This product is primarily utilized in pharmaceutical processing or compounding. It is supplied as a solution/ drops for sublingual administration. This product entry covers the primary NDC 63479-0209 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.
Primary Identification
NDC Product Code:
63479-0209
Proprietary Name:
B09 Acute Virotox
Non-Proprietary Name: [1]
Aconitum Napellus, Arsenicum Album, Baptisia Tinctoria, Belladonna, Bryonia, Cherry Plum, Clematis Vitalba, Echinacea Angustifolia, Echinacea Purpurea, Eucalyptus Globulus, Eupatorium Perfoliatum, European Olive, Ferrum Phosphoricum, Gentiana Lutea, Impatiens Glandulifera, Influenza A Virus, Lachesis Mutus, Luffa Operculata, Ornithogalum Umbellatum, Phosphorus, Rockrose, Sarcolacticum Acidum, Veratrum Album, Yellow Jasmine
Substance Name: [2]
Aconitum Napellus; Arsenic Trioxide; Atropa Belladonna; Baptisia Tinctoria Root; Bryonia Alba Root; Clematis Vitalba Flower; Echinacea Angustifolia; Echinacea Purpurea; Eucalyptus Globulus Leaf; Eupatorium Perfoliatum Flowering Top; Ferrosoferric Phosphate; Gelsemium Sempervirens Root; Gentiana Lutea Root; Helianthemum Nummularium Flower; Impatiens Glandulifera Flower; Influenza A Virus Whole; Lachesis Muta Venom; Lactic Acid, L-; Luffa Operculata Fruit; Olea Europaea Flower; Ornithogalum Umbellatum Flowering Top; Phosphorus; Prunus Cerasifera Flower; Veratrum Album Root
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:
Clinical Specifications
Dosage Form:
Solution/ Drops
- A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
Sublingual - Administration beneath the tongue.
Labeler & Regulatory Data
Labeler Name: [5]
Labeler Code:
63479
Product Label ID:
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Marketing Timeline
Start Marketing Date: [9]
12-15-1994
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N
Code Structure Chart
Product Details
What is NDC 63479-0209?
The NDC code 63479-0209 is assigned by the FDA to the product B09 Acute Virotox. It is commonly known by its generic name, aconitum napellus, arsenicum album, baptisia tinctoria, belladonna, bryonia, cherry plum, clematis vitalba, echinacea angustifolia, echinacea purpurea, eucalyptus globulus, eupatorium perfoliatum, european olive, ferrum phosphoricum, gentiana lutea, impatiens glandulifera, influenza a virus, lachesis mutus, luffa operculata, ornithogalum umbellatum, phosphorus, rockrose, sarcolacticum acidum, veratrum album, yellow jasmine. This pharmaceutical product is labeled by Apex Energetics Inc. and is currently categorized as listed product. The medication is a solution/ drops administered via sublingual route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 63479-0209-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.
What are the uses of this product?
Adults & children ages 12 years and over: Take 5-8 drops under the tongue 3-4 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.
What are Active Ingredients of this product?
An 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.
- ACONITUM NAPELLUS 200 [hp_X]/mL - A plant genus of the family RANUNCULACEAE. Members contain a number of diterpenoid alkaloids including: aconitans, hypaconitine, ACONITINE, jesaconitine, ignavine, napelline, and mesaconitine. The common name of Wolfbane is similar to the common name for ARNICA.
- ARSENIC TRIOXIDE 200 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- ATROPA BELLADONNA 200 [hp_X]/mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
- BAPTISIA TINCTORIA ROOT 9 [hp_X]/mL
- BRYONIA ALBA ROOT 200 [hp_X]/mL
- CLEMATIS VITALBA FLOWER 9 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA 1 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- ECHINACEA PURPUREA 1 [hp_X]/mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
- EUCALYPTUS GLOBULUS LEAF 12 [hp_X]/mL
- EUPATORIUM PERFOLIATUM FLOWERING TOP 3 [hp_X]/mL
- FERROSOFERRIC PHOSPHATE 200 [hp_X]/mL
- GELSEMIUM SEMPERVIRENS ROOT 30 [hp_X]/mL
- GENTIANA LUTEA ROOT 6 [hp_X]/mL
- HELIANTHEMUM NUMMULARIUM FLOWER 9 [hp_X]/mL
- IMPATIENS GLANDULIFERA FLOWER 9 [hp_X]/mL
- INFLUENZA A VIRUS WHOLE 30 [hp_X]/mL
- LACHESIS MUTA VENOM 30 [hp_X]/mL
- LACTIC ACID, L- 12 [hp_X]/mL
- LUFFA OPERCULATA FRUIT 12 [hp_X]/mL
- OLEA EUROPAEA FLOWER 9 [hp_X]/mL
- ORNITHOGALUM UMBELLATUM FLOWERING TOP 9 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- PRUNUS CERASIFERA FLOWER 9 [hp_X]/mL
- VERATRUM ALBUM ROOT 12 [hp_X]/mL
Which are the associated UNII Codes?
The UNII codes for the active ingredients in this product are:
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
- ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD)
- ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
- PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
- PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
- HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
- HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU)
- BAPTISIA TINCTORIA ROOT (UNII: 5EF0HWI5WU) (Active Moiety)
- CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI)
- CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI) (Active Moiety)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6) (Active Moiety)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B)
- BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
- FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
- ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS)
- GENTIANA LUTEA ROOT (UNII: S72O3284MS) (Active Moiety)
- IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
- IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I)
- LACHESIS MUTA VENOM (UNII: VSW71SS07I) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
- VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
- EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ)
- OLEA EUROPAEA FLOWER (UNII: 498M34P1VZ) (Active Moiety)
- INFLUENZA A VIRUS WHOLE (UNII: R9HH0NDE2E)
- INFLUENZA A VIRUS WHOLE (UNII: R9HH0NDE2E) (Active Moiety)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU)
- LUFFA OPERCULATA FRUIT (UNII: C4MO6809HU) (Active Moiety)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
- ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B)
- ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (Active Moiety)
Which are the Inactive Ingredients associated UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
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Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An 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.
What kind of product is this? Indicates 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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product 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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".
