1. Home
  2. Labeler Index
  3. Similasan Ag
  4. NDC Product Code: 53799-376 Dry Eye Relief Trial Size 15x

NDC 53799-376 Dry Eye Relief Trial Size 15x

Belladonna,Euphrasia Officinalis,Mercurius Sublimatus,Solution/ Drops Ophthalmic - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53799-376?
  4. Dry Eye Relief Trial Size 15x Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

NDC Product Code:
53799-376
Proprietary Name:
Dry Eye Relief Trial Size 15x
Non-Proprietary Name: [1]
Belladonna, Euphrasia Officinalis, Mercurius Sublimatus,
Substance Name: [2]
Atropa Belladonna; Euphrasia Stricta; Mercuric Chloride
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
  • Ophthalmic - Administration to the external eye.
    • Labeler Name: [5]
    Similasan Ag
    Labeler Code:
    53799
    Product Label ID:
    26e39619-634c-42d2-92da-44e49df85f05
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    07-08-2021
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 53799-376-01

    Package Description: 270 BOTTLE, DROPPER in 1 CARTON / .45 mL in 1 BOTTLE, DROPPER

    NDC Code 53799-376-13

    Package Description: .4 mL in 1 VIAL, SINGLE-USE

    Product Details

    What is NDC 53799-376?

    The NDC code 53799-376 is assigned by the FDA to the product Dry Eye Relief Trial Size 15x which is a human over the counter drug product labeled by Similasan Ag. The generic name of Dry Eye Relief Trial Size 15x is belladonna, euphrasia officinalis, mercurius sublimatus, . The product's dosage form is solution/ drops and is administered via ophthalmic form. The product is distributed in 2 packages with assigned NDC codes 53799-376-01 270 bottle, dropper in 1 carton / .45 ml in 1 bottle, dropper, 53799-376-13 .4 ml in 1 vial, single-use . 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 Dry Eye Relief Trial Size 15x?

    For adults and children age 2 and over:twist flat end with ball to opensqueeze plastic dropper to release 2-3 drops into eye and discard applicatorapply as needed

    What are Dry Eye Relief Trial Size 15x 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.
    • ATROPA BELLADONNA 6 [hp_X]/10mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
    • EUPHRASIA STRICTA 6 [hp_X]/10mL
    • MERCURIC CHLORIDE 15 [hp_X]/10mL - Mercury chloride (HgCl2). A highly toxic compound that volatizes slightly at ordinary temperature and appreciably at 100 degrees C. It is corrosive to mucous membranes and used as a topical antiseptic and disinfectant.
    • ATROPA BELLADONNA 6 [hp_X]/10mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
    • EUPHRASIA STRICTA 6 [hp_X]/10mL
    • MERCURIC CHLORIDE 15 [hp_X]/10mL - Mercury chloride (HgCl2). A highly toxic compound that volatizes slightly at ordinary temperature and appreciably at 100 degrees C. It is corrosive to mucous membranes and used as a topical antiseptic and disinfectant.

    Which are Dry Eye Relief Trial Size 15x UNII Codes?

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

    Which are Dry Eye Relief Trial Size 15x 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".