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NDC 59228-103 Sinofresh Nasal And Sinus Care

Eucalyptus Globulus Leaf,Potassium Dichromate Liquid Topical - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 59228-103?
  4. Sinofresh Nasal And Sinus Care Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
59228-103
Proprietary Name:
Sinofresh Nasal And Sinus Care
Non-Proprietary Name: [1]
Eucalyptus Globulus Leaf, Potassium Dichromate
Substance Name: [2]
Eucalyptus Globulus Leaf; Potassium Dichromate
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]
  • 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]
    Ems Contract Packaging
    Labeler Code:
    59228
    Product Label ID:
    e1cdfbed-54d9-452b-bf0c-d62c1b9b2c9e
    Marketing Category: [8]
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date: [9]
    05-30-2014
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
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    Code Structure Chart

    Product Details

    What is NDC 59228-103?

    The NDC code 59228-103 is assigned by the FDA to the product Sinofresh Nasal And Sinus Care which is a human over the counter drug product labeled by Ems Contract Packaging. The generic name of Sinofresh Nasal And Sinus Care is eucalyptus globulus leaf, potassium dichromate. The product's dosage form is liquid and is administered via topical form. The product is distributed in a single package with assigned NDC code 59228-103-11 29.6 ml in 1 bottle . 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 Sinofresh Nasal And Sinus Care?

    USESRELIEVES NASAL AND SINUS SYMPTOMS ASSOCIATED WITH PERSISTENT SINUS CONDITIONS:CONGESTIONNASAL INFLAMMATIONSINUS PRESSUREFACIAL PINSINUS HEADACHESTUFFY NOSE

    What are Sinofresh Nasal And Sinus Care 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.
    • EUCALYPTUS GLOBULUS LEAF 20 [hp_X]/100mL
    • POTASSIUM DICHROMATE 30 [hp_X]/100mL - Chromic acid (H2Cr2O7), dipotassium salt. A compound having bright orange-red crystals and used in dyeing, staining, tanning leather, as bleach, oxidizer, depolarizer for dry cells, etc. Medically it has been used externally as an astringent, antiseptic, and caustic. When taken internally, it is a corrosive poison.

    Which are Sinofresh Nasal And Sinus Care UNII Codes?

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

    Which are Sinofresh Nasal And Sinus Care 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:

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    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".