NDC 17312-013 Pink Eye Relief

Aconitum Napellus - Apis Mellifera - Silver Nitrate - Euphrasia Stricta - Sodium - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
17312-013
Proprietary Name:
Pink Eye Relief
Non-Proprietary Name: [1]
Aconitum Napellus - Apis Mellifera - Silver Nitrate - Euphrasia Stricta - Sodium Arsenate, Dibasic, Heptahydrate -
Substance Name: [2]
Aconitum Napellus; Apis Mellifera; Euphrasia Stricta; Silver Nitrate; Sodium Arsenate, Dibasic, Heptahydrate
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]
  • Ophthalmic - Administration to the external eye.
  • Labeler Name: [5]
    Trp Company
    Labeler Code:
    17312
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    09-01-2012
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 17312-013-15

    Package Description: 1 BOTTLE, DROPPER in 1 PACKAGE / 10 mL in 1 BOTTLE, DROPPER

    NDC Code 17312-013-99

    Package Description: 1 BOTTLE, DROPPER in 1 PACKAGE / 2.5 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 17312-013?

    The NDC code 17312-013 is assigned by the FDA to the product Pink Eye Relief which is a human over the counter drug product labeled by Trp Company. The generic name of Pink Eye Relief is aconitum napellus - apis mellifera - silver nitrate - euphrasia stricta - sodium arsenate, dibasic, heptahydrate -. The product's dosage form is liquid and is administered via ophthalmic form. The product is distributed in 2 packages with assigned NDC codes 17312-013-15 1 bottle, dropper in 1 package / 10 ml in 1 bottle, dropper, 17312-013-99 1 bottle, dropper in 1 package / 2.5 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 Pink Eye Relief?

    Uses:* According to homeopathic indications these ingredients temporarily relieve minor symptoms such as: • Redness • Burning sensations • Watering • Swelling • Inflammation • Sensation of grittiness and overnight crusting after serious causes have been ruled out by a physician. *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

    What are Pink Eye 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 Pink Eye Relief UNII Codes?

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

    Which are Pink Eye 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 Pink Eye 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".