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  5. NDC Package Code: 16030-501-05 Carboxymethylcellulose Sodium Eye Drops 0.5%

NDC Package 16030-501-05 Carboxymethylcellulose Sodium Eye Drops 0.5%

For Solution Topical - 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:
16030-501-05
Package Description:
5 mL in 1 BOTTLE, DROPPER
Product Code:
16030-501
Proprietary Name:
Carboxymethylcellulose Sodium Eye Drops 0.5%
Non-Proprietary Name:
Carboxymethylcellulose Sodium Eye Drops 0.5%
Substance Name:
Carboxymethylcellulose Sodium, Unspecified
Usage Information:
Lnstill 1or 2 drops in the affected eye, as needed
11-Digit NDC Billing Format:
16030050105
NDC to RxNorm Crosswalk:
  • RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 % Ophthalmic Solution
  • RxCUI: 1188426 - carboxymethylcellulose sodium 5 MG/ML Ophthalmic Solution
  • RxCUI: 1188426 - carboxymethylcellulose sodium 0.5 GM per 100 ML Ophthalmic Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Aurolab
    Dosage Form:
    For Solution - A product, usually a solid, intended for solution prior to administration.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED 5 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    part349
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    09-20-2022
    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 16030-501-05?

    The NDC Packaged Code 16030-501-05 is assigned to a package of 5 ml in 1 bottle, dropper of Carboxymethylcellulose Sodium Eye Drops 0.5%, a human over the counter drug labeled by Aurolab. The product's dosage form is for solution and is administered via topical form.

    Is NDC 16030-501 included in the NDC Directory?

    Yes, Carboxymethylcellulose Sodium Eye Drops 0.5% with product code 16030-501 is active and included in the NDC Directory. The product was first marketed by Aurolab on September 20, 2022 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 16030-501-05?

    The 11-digit format is 16030050105. 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
    5-3-216030-501-055-4-216030-0501-05