NDC 63479-0220 B20 Acute Rescue

Aconitum Napellus,Apis Mellifica,Arnica Montana,Arsenicum Album,Belladonna,Bellis - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
63479-0220
Proprietary Name:
B20 Acute Rescue
Non-Proprietary Name: [1]
Aconitum Napellus, Apis Mellifica, Arnica Montana, Arsenicum Album, Belladonna, Bellis Perennis, Bryonia, Calendula, Chamomilla, Cherry Plum, Clematis Vitalba, Colocynthis, Dulcamara Lignosa, Echinacea, Eupatorium, Ferrum Phosphoricum, Hamamelis Virginiana, Histaminum, Hypericum Perforatum, Impatiens Glandulifera, Ledum Palustre, Mentha Piperita, Millefolium, Plantago Major, Pyrenees Star Of Bethlehem, Rhus Toxicodendron, Rockrose, Sulfur, Comfrey, Veratrum Album, Verbascum Thapsus
Substance Name: [2]
Achillea Millefolium; Aconitum Napellus Whole; Apis Mellifera; Arnica Montana; Arsenic Trioxide; Atropa Belladonna; Bellis Perennis; Bryonia Alba Root; Calendula Officinalis Flowering Top; Citrullus Colocynthis Fruit Pulp; Clematis Vitalba Flower; Comfrey Root; Echinacea Angustifolia; Echinacea Purpurea; Eupatorium Perfoliatum Flowering Top; Ferrosoferric Phosphate; Hamamelis Virginiana Root Bark/stem Bark; Helianthemum Nummularium Flower; Histamine Dihydrochloride; Hypericum Perforatum; Impatiens Glandulifera Flower; Matricaria Chamomilla; Mentha Piperita; Ornithogalum Umbellatum Flowering Top; Plantago Major; Prunus Cerasifera Flower; Rhododendron Tomentosum Leafy Twig; Solanum Dulcamara Whole; Sulfur; Toxicodendron Pubescens Leaf; Veratrum Album Root; Verbascum Thapsus
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s): [4]
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • Labeler Name: [5]
    Apex Energetics Inc.
    Labeler Code:
    63479
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    08-30-1994
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 63479-0220-1

    Package Description: 50 mL in 1 BOTTLE, PUMP

    Product Details

    What is NDC 63479-0220?

    The NDC code 63479-0220 is assigned by the FDA to the product B20 Acute Rescue which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of B20 Acute Rescue is aconitum napellus, apis mellifica, arnica montana, arsenicum album, belladonna, bellis perennis, bryonia, calendula, chamomilla, cherry plum, clematis vitalba, colocynthis, dulcamara lignosa, echinacea, eupatorium, ferrum phosphoricum, hamamelis virginiana, histaminum, hypericum perforatum, impatiens glandulifera, ledum palustre, mentha piperita, millefolium, plantago major, pyrenees star of bethlehem, rhus toxicodendron, rockrose, sulfur, comfrey, veratrum album, verbascum thapsus. The product's dosage form is cream and is administered via topical form. The product is distributed in a single package with assigned NDC code 63479-0220-1 50 ml in 1 bottle, pump . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for B20 Acute Rescue?

    Adults & children ages 12 years and over: Apply one pump topically to affected area not more than 5 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

    What are B20 Acute Rescue Active Ingredients?

    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.

    Which are B20 Acute Rescue UNII Codes?

    The UNII codes for the active ingredients in this product are:

    • PLANTAGO MAJOR (UNII: W2469WNO6U)
    • PLANTAGO MAJOR (UNII: W2469WNO6U) (Active Moiety)
    • ARNICA MONTANA (UNII: O80TY208ZW)
    • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
    • ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
    • ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
    • CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ) (Active Moiety)
    • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
    • MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ) (Active Moiety)
    • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI)
    • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI) (Active Moiety)
    • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17)
    • CITRULLUS COLOCYNTHIS FRUIT PULP (UNII: 23H32AOH17) (Active Moiety)
    • SOLANUM DULCAMARA WHOLE (UNII: G72JA9DHK5)
    • SOLANUM DULCAMARA WHOLE (UNII: G72JA9DHK5) (Active Moiety)
    • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)
    • ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (Active Moiety)
    • HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
    • HISTAMINE (UNII: 820484N8I3) (Active Moiety)
    • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B)
    • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (Active Moiety)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A)
    • TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (Active Moiety)
    • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
    • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
    • SULFUR (UNII: 70FD1KFU70)
    • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
    • VERBASCUM THAPSUS (UNII: C9TD27U172)
    • VERBASCUM THAPSUS (UNII: C9TD27U172) (Active Moiety)
    • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD)
    • ACONITUM NAPELLUS WHOLE (UNII: U0NQ8555JD) (Active Moiety)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (Active Moiety)
    • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
    • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
    • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
    • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
    • MENTHA PIPERITA (UNII: 79M2M2UDA9)
    • MENTHA PIPERITA (UNII: 79M2M2UDA9) (Active Moiety)
    • APIS MELLIFERA (UNII: 7S82P3R43Z)
    • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (Active Moiety)
    • ECHINACEA PURPUREA (UNII: QI7G114Y98)
    • ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
    • RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P)
    • RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P) (Active Moiety)
    • COMFREY ROOT (UNII: M9VVZ08EKQ)
    • COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
    • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
    • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)
    • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7)
    • FERROSOFERRIC PHOSPHATE (UNII: 91GQH8I5F7) (Active Moiety)
    • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS)
    • HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK (UNII: T7S323PKJS) (Active Moiety)
    • BELLIS PERENNIS (UNII: 2HU33I03UY)
    • BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (Active Moiety)

    Which are B20 Acute Rescue Inactive Ingredients 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:

    Which are the Pharmacologic Classes for B20 Acute Rescue?

    A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

    * Please review the disclaimer below.

    Product Footnotes

    [1] 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.

    [2] 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.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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.

    [12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".