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  4. NDC Product Code: 43857-0532 Sinus Tonic

NDC 43857-0532 Sinus Tonic

Echinacea (angustifolia),Baptisia Tinctoria,Thiaminum Hydrochloricum,Hydrastis - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0532?
  4. Sinus Tonic Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
43857-0532
Proprietary Name:
Sinus Tonic
Non-Proprietary Name: [1]
Echinacea (angustifolia), Baptisia Tinctoria, Thiaminum Hydrochloricum, Hydrastis Canadensis, Pyridoxinum Hydrochloricum, Spongia Tosta, Apis Mellifica, Ascorbic Acid, Hepar Sulphuris Calcareum, Kali Bichromicum, Lachesis Mutus, Mercurius Iodatus Ruber, Mercurius Sulphuratus Ruber, Pulsatilla (pratensis), Silicea, Sinusitisinum, Pantothenic Acid
Substance Name: [2]
Apis Mellifera; Ascorbic Acid; Baptisia Tinctoria Root; Calcium Sulfide; Echinacea Angustifolia Whole; Goldenseal; Lachesis Muta Venom; Mercuric Iodide; Mercuric Sulfide; Pantothenic Acid; Potassium Dichromate; Pulsatilla Pratensis Whole; Pyridoxine Hydrochloride; Silicon Dioxide; Sinusitisinum; Spongia Officinalis Skeleton, Roasted; Thiamine Hydrochloride
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
    • Labeler Name: [5]
    Bioactive Nutritional, Inc.
    Labeler Code:
    43857
    Product Label ID:
    63234fdc-7456-42c6-8996-fef372dd4a53
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    01-02-2020
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 43857-0532-1

    Package Description: 60 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 43857-0532?

    The NDC code 43857-0532 is assigned by the FDA to the product Sinus Tonic which is a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Sinus Tonic is echinacea (angustifolia), baptisia tinctoria, thiaminum hydrochloricum, hydrastis canadensis, pyridoxinum hydrochloricum, spongia tosta, apis mellifica, ascorbic acid, hepar sulphuris calcareum, kali bichromicum, lachesis mutus, mercurius iodatus ruber, mercurius sulphuratus ruber, pulsatilla (pratensis), silicea, sinusitisinum, pantothenic acid. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 43857-0532-1 60 ml in 1 bottle, dropper . 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 Sinus Tonic?

    For temporary relief of redness and swelling of the nasal passages with post nasal drip, thick, yellowish discharge from the nose, foul smell; frequent coryza alternating with stoppage. For temporary relief of redness and swelling of the nasal passages with post nasal drip, thick, yellowish discharge from the nose, foul smell; frequent coryza alternating with stoppage.

    What are Sinus Tonic 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 Sinus Tonic UNII Codes?

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

    Which are Sinus Tonic 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".