NDC Package 79481-0250-1 Meijer Multi-symptom Relief

Polyethylene Glycol 400,Tetrahydrozoline Hcl,Zinc Sulfate Solution/ Drops Ophthalmic - 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:
79481-0250-1
Package Description:
1 BOTTLE, DROPPER in 1 CARTON / 15 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Meijer Multi-symptom Relief
Non-Proprietary Name:
Polyethylene Glycol 400, Tetrahydrozoline Hcl, Zinc Sulfate
Substance Name:
Polyethylene Glycol 400; Tetrahydrozoline Hydrochloride; Zinc Sulfate
Usage Information:
UsesRelieves dryness of the eyefor temporary relief of discomfort and redness of the eye due to minor eye irritationsfor temporary relief of burning and irritation due to exposure to wind or sunfor protection against further irritation
11-Digit NDC Billing Format:
79481025001
NDC to RxNorm Crosswalk:
  • RxCUI: 2360903 - polyethylene glycol 400 1 % / tetrahydrozoline hydrochloride 0.05 % / zinc sulfate 0.25 % Ophthalmic Solution
  • RxCUI: 2360903 - polyethylene glycol 400 10 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic Solution
  • RxCUI: 2360903 - polyethylene glycol 400 10 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML / ZnSO4 2.5 MG/ML Ophthalmic Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Meijer, Inc.
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Sample Package:
    No
    FDA Application Number:
    M018
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-09-2023
    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.

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    Frequently Asked Questions

    What is NDC 79481-0250-1?

    The NDC Packaged Code 79481-0250-1 is assigned to a package of 1 bottle, dropper in 1 carton / 15 ml in 1 bottle, dropper of Meijer Multi-symptom Relief, a human over the counter drug labeled by Meijer, Inc.. The product's dosage form is solution/ drops and is administered via ophthalmic form.

    Is NDC 79481-0250 included in the NDC Directory?

    Yes, Meijer Multi-symptom Relief with product code 79481-0250 is active and included in the NDC Directory. The product was first marketed by Meijer, Inc. on January 09, 2023 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 79481-0250-1?

    The 11-digit format is 79481025001. 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 5-4-1 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
    5-4-179481-0250-15-4-279481-0250-01