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  5. NDC Package Code: 59262-375-12 Dry Eye Relief

NDC Package 59262-375-12 Dry Eye Relief

Atropa Belladonna And Euphrasia Stricta And Mercuric Chloride Solution/ Drops Ophthalmic - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
59262-375-12
Package Description:
20 VIAL, SINGLE-USE in 1 CARTON / .4 mL in 1 VIAL, SINGLE-USE
Product Code:
59262-375
Proprietary Name:
Dry Eye Relief
Non-Proprietary Name:
Atropa Belladonna And Euphrasia Stricta And Mercuric Chloride
Substance Name:
Atropa Belladonna; Euphrasia Stricta; Mercuric Chloride
Usage Information:
This medication is used to relieve dry, irritated eyes. Common causes for dry eyes include wind, sun, heating/air conditioning, computer use/reading, and certain medications. This product may contain 1 or more of the following ingredients: carboxymethylcellulose, dextran, glycerin, hypromellose, polyethylene glycol 400 (PEG 400), polysorbate, polyvinyl alcohol, povidone, or propylene glycol, among others. Eye lubricants keep the eye moist, help to protect the eye from injury and infection, and decrease symptoms of dry eyes such as burning, itching, and feeling as if something is in the eye.
11-Digit NDC Billing Format:
59262037512
Product Type:
Human Otc Drug
Labeler Name:
Similasan Corporation
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s):
  • Ophthalmic - Administration to the external eye.
    • Active Ingredient(s):
  • ATROPA BELLADONNA 6 [hp_X]/.4mL
  • EUPHRASIA STRICTA 6 [hp_X]/.4mL
  • MERCURIC CHLORIDE 15 [hp_X]/.4mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    03-01-2019
    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 59262-375-12?

    The NDC Packaged Code 59262-375-12 is assigned to a package of 20 vial, single-use in 1 carton / .4 ml in 1 vial, single-use of Dry Eye Relief, a human over the counter drug labeled by Similasan Corporation. The product's dosage form is solution/ drops and is administered via ophthalmic form.

    Is NDC 59262-375 included in the NDC Directory?

    Yes, Dry Eye Relief with product code 59262-375 is active and included in the NDC Directory. The product was first marketed by Similasan Corporation on March 01, 2019 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 59262-375-12?

    The 11-digit format is 59262037512. 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
    5-3-259262-375-125-4-259262-0375-12