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  5. NDC Package Code: 46122-757-37 Nighttime Relief Lubricant

NDC Package 46122-757-37 Nighttime Relief Lubricant

Light Mineral Oil,White Petrolatum Ointment 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:
46122-757-37
Package Description:
1 TUBE in 1 BOX / 3.5 g in 1 TUBE
Product Code:
46122-757
Proprietary Name:
Nighttime Relief Lubricant
Non-Proprietary Name:
Light Mineral Oil, White Petrolatum
Substance Name:
Light Mineral Oil; White Petrolatum
Usage Information:
Pull down the lower lid of the affected eyeapply a small amount (1/4 inch) of ointment to the inside of eyelid
11-Digit NDC Billing Format:
46122075737
NDC to RxNorm Crosswalk:
  • RxCUI: 702008 - mineral oil 42.5 % / petrolatum 57.3 % Ophthalmic Ointment
  • RxCUI: 702008 - mineral oil 0.425 MG/MG / petrolatum 0.573 MG/MG Ophthalmic Ointment
  • RxCUI: 702008 - mineral oil 42.5 % / petrolatum, white 57.3 % Ophthalmic Ointment
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Amerisource Bergen Drug Corp.
    Dosage Form:
    Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
    • Active Ingredient(s):
  • LIGHT MINERAL OIL 425 mg/g
  • WHITE PETROLATUM 573 mg/g
    • Sample Package:
    No
    FDA Application Number:
    M018
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-05-2023
    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.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 46122-757-37?

    The NDC Packaged Code 46122-757-37 is assigned to a package of 1 tube in 1 box / 3.5 g in 1 tube of Nighttime Relief Lubricant, a human over the counter drug labeled by Amerisource Bergen Drug Corp.. The product's dosage form is ointment and is administered via ophthalmic form.

    Is NDC 46122-757 included in the NDC Directory?

    Yes, Nighttime Relief Lubricant with product code 46122-757 is active and included in the NDC Directory. The product was first marketed by Amerisource Bergen Drug Corp. on June 05, 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 46122-757-37?

    The 11-digit format is 46122075737. 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
    5-3-246122-757-375-4-246122-0757-37