NDC Package 17312-039-15 Eye Floaters Relief

Chelidonium Majus,Physostigma Venenosum Seed,Euphrasia Stricta, Potassium Sulfate,Sodium - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
17312-039-15
Package Description:
1 BOTTLE, DROPPER in 1 PACKAGE / 10 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Eye Floaters Relief
Non-Proprietary Name:
Chelidonium Majus, Physostigma Venenosum Seed, Euphrasia Stricta, Potassium Sulfate, Sodium Chloride, Phosphorus, Silicon Dioxide, Sepia Officinalis Juice
Substance Name:
Chelidonium Majus; Euphrasia Stricta; Phosphorus; Physostigma Venenosum Seed; Potassium Sulfate; Sepia Officinalis Juice; Silicon Dioxide; Sodium Chloride
Usage Information:
Uses:* According to homeopathic indications these ingredients provide temporary relief from symptoms such as: • Floaters • Squiggly lines in vision • Irritation • Dark dots in vision • Shapes in vision • Dust particles in vision; 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.
11-Digit NDC Billing Format:
17312003915
Product Type:
Human Otc Drug
Labeler Name:
Trp Company
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):
  • Ophthalmic - Administration to the external eye.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    05-28-2018
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17312-039-15?

    The NDC Packaged Code 17312-039-15 is assigned to a package of 1 bottle, dropper in 1 package / 10 ml in 1 bottle, dropper of Eye Floaters Relief, a human over the counter drug labeled by Trp Company. The product's dosage form is liquid and is administered via ophthalmic form.

    Is NDC 17312-039 included in the NDC Directory?

    Yes, Eye Floaters Relief with product code 17312-039 is active and included in the NDC Directory. The product was first marketed by Trp Company on May 28, 2018 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17312-039-15?

    The 11-digit format is 17312003915. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-217312-039-155-4-217312-0039-15