NDC Package 10742-8146-1 Rohto All-in-one

Hypromellose,Tetrahydrozoline Hydrochloride,Zinc Sulfate Liquid 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:
10742-8146-1
Package Description:
1 BOTTLE, WITH APPLICATOR in 1 CARTON / 13 mL in 1 BOTTLE, WITH APPLICATOR
Product Code:
Proprietary Name:
Rohto All-in-one
Non-Proprietary Name:
Hypromellose, Tetrahydrozoline Hydrochloride, Zinc Sulfate
Substance Name:
Hypromellose, Unspecified; Tetrahydrozoline Hydrochloride; Zinc Sulfate, Unspecified Form
Usage Information:
•put 1 or 2 drops in the affected eye(s) up to 4 times daily•tightly snap on cap to sealOther information•store at 20-25°C (68-77°F)
11-Digit NDC Billing Format:
10742814601
NDC to RxNorm Crosswalk:
  • RxCUI: 1098640 - hypromellose 0.2 % / tetrahydrozoline HCl 0.05 % / zinc sulfate 0.25 % Ophthalmic Solution
  • RxCUI: 1098640 - hypromellose 2 MG/ML / tetrahydrozoline hydrochloride 0.5 MG/ML / zinc sulfate 2.5 MG/ML Ophthalmic Solution
  • RxCUI: 1098640 - hypromellose 0.2 % / tetrahydrozoline hydrochloride 0.05 % / zinc sulfate 0.25 % Ophthalmic Solution
  • RxCUI: 1098640 - hypromellose 2 MG/ML / Tetrahydrozoline hydrochloride 0.5 MG/ML / ZnSO4 2.5 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.
  • 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:
    06-21-2021
    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 10742-8146-1?

    The NDC Packaged Code 10742-8146-1 is assigned to a package of 1 bottle, with applicator in 1 carton / 13 ml in 1 bottle, with applicator of Rohto All-in-one, 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 10742-8146 included in the NDC Directory?

    Yes, Rohto All-in-one with product code 10742-8146 is active and included in the NDC Directory. The product was first marketed by The Mentholatum Company on June 21, 2021 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 10742-8146-1?

    The 11-digit format is 10742814601. 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
    5-4-110742-8146-15-4-210742-8146-01