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  4. NDC Product Code: 63479-0201 B01 Acute Rescue

NDC 63479-0201 B01 Acute Rescue

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

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63479-0201?
  4. B01 Acute Rescue Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
63479-0201
Proprietary Name:
B01 Acute Rescue
Non-Proprietary Name: [1]
Aconitum Napellus, Apis Mellifica, Arnica Montana, Arsenicum Album, Belladonna, Bellis Perennis, Bryonia Alba, Calendula Officinalis, Chamomilla, Cherry Plum, Clematis, Colocynthis, Dulcamara, Echinacea Angustifolia, Echinacea Purpurea, Eupatorium Perfoliatum, Ferrum Phosphoricum, Hamamelis Virginiana, Histaminum, Hypericum Perforatum, Impatiens, Millefolium, Rhus Toxicodendron, Rock Rose, Star Of Bethlehem, Sulphur, Symphytum Officinale, Veratrum Album
Substance Name: [2]
Achillea Millefolium; Aconitum Napellus; 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; Ornithogalum Umbellatum Flowering Top; Prunus Cerasifera Flower; Solanum Dulcamara Whole; Sulfur; Toxicodendron Pubescens Leaf; Veratrum Album Root
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s): [4]
  • Sublingual - Administration beneath the tongue.
    • Labeler Name: [5]
    Apex Energetics Inc.
    Labeler Code:
    63479
    Product Label ID:
    4ce96ca9-8964-4b60-9d99-bf01d3d1cb43
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    08-15-1988
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 63479-0201?

    The NDC code 63479-0201 is assigned by the FDA to the product B01 Acute Rescue which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of B01 Acute Rescue is aconitum napellus, apis mellifica, arnica montana, arsenicum album, belladonna, bellis perennis, bryonia alba, calendula officinalis, chamomilla, cherry plum, clematis, colocynthis, dulcamara, echinacea angustifolia, echinacea purpurea, eupatorium perfoliatum, ferrum phosphoricum, hamamelis virginiana, histaminum, hypericum perforatum, impatiens, millefolium, rhus toxicodendron, rock rose, star of bethlehem, sulphur, symphytum officinale, veratrum album. The product's dosage form is solution and is administered via sublingual form. The product is distributed in a single package with assigned NDC code 63479-0201-1 30 ml in 1 bottle, glass . 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 B01 Acute Rescue?

    Adults & children ages 12 years and over: Take 10 drops under the tongue 1-3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

    What are B01 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 B01 Acute Rescue UNII Codes?

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

    • ACONITUM NAPELLUS (UNII: U0NQ8555JD)
    • ACONITUM NAPELLUS (UNII: U0NQ8555JD) (Active Moiety)
    • APIS MELLIFERA (UNII: 7S82P3R43Z)
    • APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
    • ARNICA MONTANA (UNII: O80TY208ZW)
    • ARNICA MONTANA (UNII: O80TY208ZW) (Active Moiety)
    • ARNICA MONTANA ROOT (UNII: MUE8Y11327) (Active Moiety)
    • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
    • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
    • ATROPA BELLADONNA (UNII: WQZ3G9PF0H)
    • ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (Active Moiety)
    • BELLIS PERENNIS (UNII: 2HU33I03UY)
    • BELLIS PERENNIS (UNII: 2HU33I03UY) (Active Moiety)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B)
    • BRYONIA ALBA ROOT (UNII: T7J046YI2B) (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)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (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)
    • ECHINACEA PURPUREA (UNII: QI7G114Y98)
    • ECHINACEA PURPUREA (UNII: QI7G114Y98) (Active Moiety)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E)
    • EUPATORIUM PERFOLIATUM FLOWERING TOP (UNII: 1W0775VX6E) (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)
    • HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
    • HISTAMINE (UNII: 820484N8I3) (Active Moiety)
    • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB)
    • HYPERICUM PERFORATUM (UNII: XK4IUX8MNB) (Active Moiety)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK)
    • ACHILLEA MILLEFOLIUM (UNII: 2FXJ6SW4PK) (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)
    • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B)
    • ORNITHOGALUM UMBELLATUM FLOWERING TOP (UNII: CZD6M4PY4B) (Active Moiety)
    • SULFUR (UNII: 70FD1KFU70)
    • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
    • COMFREY ROOT (UNII: M9VVZ08EKQ)
    • COMFREY ROOT (UNII: M9VVZ08EKQ) (Active Moiety)
    • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z)
    • VERATRUM ALBUM ROOT (UNII: QNS6W5US1Z) (Active Moiety)

    Which are B01 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 B01 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".