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  5. NDC Package Code: 66051-236-80 Eyewash Additive Concentrate

NDC Package 66051-236-80 Eyewash Additive Concentrate

Water And Propylene Glycol Liquid 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:
66051-236-80
Package Description:
.236 L in 1 BOTTLE, UNIT-DOSE
Product Code:
66051-236
Proprietary Name:
Eyewash Additive Concentrate
Non-Proprietary Name:
Water And Propylene Glycol
Substance Name:
Propylene Glycol; Water
Usage Information:
Wear protective eyewear and glovesclean potable eyewash station and rinse with potable waterpartially fill station with potable waterremove tamper evident seal and cap of bottleadd entire contents of the bottle to the eyewash station containerfill the station to the manufacturer’s required leveldate and initial inspection tagstation should be cleaned and refilled every 120 days when using this productin advance of emergency, add the concentrate to potable water to have a solution available
11-Digit NDC Billing Format:
66051023680
Product Type:
Human Otc Drug
Labeler Name:
Haws Corporation
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.
    • Active Ingredient(s):
  • PROPYLENE GLYCOL 280 kg/2800L
  • WATER 2374.4 L/2800L
    • Sample Package:
    No
    FDA Application Number:
    M018
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    07-02-2019
    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 66051-236-80?

    The NDC Packaged Code 66051-236-80 is assigned to a package of .236 l in 1 bottle, unit-dose of Eyewash Additive Concentrate, a human over the counter drug labeled by Haws Corporation. The product's dosage form is liquid and is administered via ophthalmic form.

    Is NDC 66051-236 included in the NDC Directory?

    Yes, Eyewash Additive Concentrate with product code 66051-236 is active and included in the NDC Directory. The product was first marketed by Haws Corporation on July 02, 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 66051-236-80?

    The 11-digit format is 66051023680. 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
    5-3-266051-236-805-4-266051-0236-80