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  5. NDC Package Code: 10742-8161-1 Rohto Preservative Free Dry Aid

NDC Package 10742-8161-1 Rohto Preservative Free Dry Aid

Povidone,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:
10742-8161-1
Package Description:
30 VIAL, SINGLE-USE in 1 CARTON / .5 mL in 1 VIAL, SINGLE-USE
Product Code:
10742-8161
Proprietary Name:
Rohto Preservative Free Dry Aid
Non-Proprietary Name:
Povidone, Propylene Glycol
Substance Name:
Povidone, Unspecified; Propylene Glycol
Usage Information:
•twist tab completely to remove; do not pull tab off•instill 1 or 2 drops in the affected eye(s) as needed•discard containerOther information•use only if single-use container is intact•do not freeze
11-Digit NDC Billing Format:
10742816101
NDC to RxNorm Crosswalk:
  • RxCUI: 1863574 - povidone 0.68 % / propylene glycol 0.3 % Opthalmic Solution
  • RxCUI: 1863574 - povidone 6.8 MG/ML / propylene glycol 3 MG/ML Ophthalmic Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    The Mentholatum Company
    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):
  • POVIDONE, UNSPECIFIED 6.8 mg/mL
  • PROPYLENE GLYCOL 3 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:
    06-03-2022
    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 10742-8161-1?

    The NDC Packaged Code 10742-8161-1 is assigned to a package of 30 vial, single-use in 1 carton / .5 ml in 1 vial, single-use of Rohto Preservative Free Dry Aid, a human over the counter drug labeled by The Mentholatum Company. The product's dosage form is liquid and is administered via ophthalmic form.

    Is NDC 10742-8161 included in the NDC Directory?

    Yes, Rohto Preservative Free Dry Aid with product code 10742-8161 is active and included in the NDC Directory. The product was first marketed by The Mentholatum Company on June 03, 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 10742-8161-1?

    The 11-digit format is 10742816101. 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
    5-4-110742-8161-15-4-210742-8161-01