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NDC 68703-345 Cough And Cold Relief

Arg Met,Arsenicum Alb,Baptisia,Bryonia,Causticum,Dulcamara,Echinacea - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 68703-345?
  4. Cough And Cold Relief Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
68703-345
Proprietary Name:
Cough And Cold Relief
Non-Proprietary Name: [1]
Arg Met, Arsenicum Alb, Baptisia, Bryonia, Causticum, Dulcamara, Echinacea Angustifolia, Echinacea Purp, Kali Bic, Merc Coros, Phos, Pulsatilla Nutt, Senega, Zinc Pic, Zinc Val
Substance Name: [2]
Anemone Patens Whole; Arsenic Trioxide; Baptisia Tinctoria; Causticum; Echinacea Angustifolia; Echinacea Purpurea; Mercuric Chloride; Phosphorus; Polygala Senega Root; Potassium Chloride; Potassium Dichromate; Silver; Solanum Dulcamara Flower; Zinc Picrate; Zinc Valerate
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Spray - A liquid minutely divided as by a jet of air or steam.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Silver Star Brands
    Labeler Code:
    68703
    Product Label ID:
    9d4a851c-ebda-1918-e053-2995a90a4936
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    10-01-2019
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
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    Product Details

    What is NDC 68703-345?

    The NDC code 68703-345 is assigned by the FDA to the product Cough And Cold Relief which is a human over the counter drug product labeled by Silver Star Brands. The generic name of Cough And Cold Relief is arg met, arsenicum alb, baptisia, bryonia, causticum, dulcamara, echinacea angustifolia, echinacea purp, kali bic, merc coros, phos, pulsatilla nutt, senega, zinc pic, zinc val. The product's dosage form is spray and is administered via oral form. The product is distributed in a single package with assigned NDC code 68703-345-02 59 ml in 1 bottle, spray . 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 Cough And Cold Relief?

    Directions: Initially, depress pump until primed. Hold close to mouth and spray directly into mouth. Adults and Children 12+: 3 sprays, 3 times per day. childeren 2-12: 2 sprays, 3 times perday. Use additionally as needed, up to 6 times per day.

    What are Cough And Cold Relief 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 Cough And Cold Relief UNII Codes?

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

    Which are Cough And Cold Relief 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 Cough And Cold Relief?

    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".