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  4. NDC Product Code: 57687-240 Rescue

NDC 57687-240 Rescue

Helianthemum Nummularium Flower,Clematis Vitalba Flower,Impatiens Glandulifera - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 57687-240?
  4. Rescue Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
57687-240
Proprietary Name:
Rescue
Non-Proprietary Name: [1]
Helianthemum Nummularium Flower, Clematis Vitalba Flower, Impatiens Glandulifera Flower, Prunus Cerasifera Flower, Ornithogalum Umbellatum, And Malus Domestica Flower
Substance Name: [2]
Clematis Vitalba Flower; Helianthemum Nummularium Flower; Impatiens Glandulifera Flower; Malus Domestica Flower; Ornithogalum Umbellatum Whole; Prunus Cerasifera Flower
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]
    Nelson Bach Usa, Ltd.
    Labeler Code:
    57687
    Product Label ID:
    c25d3cde-b80d-425a-9259-a1862cedf8e3
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-01-2009
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 57687-240-30

    Package Description: 1 TUBE in 1 CARTON / 30 g in 1 TUBE

    Product Details

    What is NDC 57687-240?

    The NDC code 57687-240 is assigned by the FDA to the product Rescue which is a human over the counter drug product labeled by Nelson Bach Usa, Ltd.. The generic name of Rescue is helianthemum nummularium flower, clematis vitalba flower, impatiens glandulifera flower, prunus cerasifera flower, ornithogalum umbellatum, and malus domestica flower. 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 57687-240-30 1 tube in 1 carton / 30 g in 1 tube. 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 Rescue?

    Clean affected area, then apply a generous amount of RESCUE® Cream to the desired area. Re-apply as required. Check that seal is intact before first use. When first opening the tube, peel off foil seal on end of tube.

    What are 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 Rescue UNII Codes?

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

    • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP)
    • HELIANTHEMUM NUMMULARIUM FLOWER (UNII: 51BRR32WPP) (Active Moiety)
    • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI)
    • CLEMATIS VITALBA FLOWER (UNII: 7SCP4N87CI) (Active Moiety)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV)
    • IMPATIENS GLANDULIFERA FLOWER (UNII: AJU5O1A5ZV) (Active Moiety)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS)
    • PRUNUS CERASIFERA FLOWER (UNII: 0KD7R09EAS) (Active Moiety)
    • ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S)
    • ORNITHOGALUM UMBELLATUM (UNII: 9NS3M2Y78S) (Active Moiety)
    • MALUS DOMESTICA FLOWER (UNII: EF626V855K)
    • MALUS DOMESTICA FLOWER (UNII: EF626V855K) (Active Moiety)

    Which are 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:

    * 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".