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  5. NDC Package Code: 55910-346-79 Rexall Maximum Strength

NDC Package 55910-346-79 Rexall Maximum Strength

Benzocaine Liquid Oral - 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:
55910-346-79
Package Description:
1 BOTTLE in 1 CARTON / 14.7 mL in 1 BOTTLE
Product Code:
55910-346
Proprietary Name:
Rexall Maximum Strength
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
Adults and children 2 years of age and older: apply to affect4ed area using applicator tipuse up to 4 times daily or as directed by a dentist or doctor. Children under 12 years of age should be supervised in the use of this product.Children under 2 years of age: ask a dentist or doctor.
11-Digit NDC Billing Format:
55910034679
NDC to RxNorm Crosswalk:
  • RxCUI: 308657 - benzocaine 20 % Mucous Membrane Topical Solution
  • RxCUI: 308657 - benzocaine 200 MG/ML Mucous Membrane Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Rexall
    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):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • BENZOCAINE 20 g/100mL
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M022
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-01-2015
    Listing Expiration Date:
    12-31-2025
    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 55910-346-79?

    The NDC Packaged Code 55910-346-79 is assigned to a package of 1 bottle in 1 carton / 14.7 ml in 1 bottle of Rexall Maximum Strength, a human over the counter drug labeled by Rexall. The product's dosage form is liquid and is administered via oral form.

    Is NDC 55910-346 included in the NDC Directory?

    Yes, Rexall Maximum Strength with product code 55910-346 is active and included in the NDC Directory. The product was first marketed by Rexall on January 01, 2015 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 55910-346-79?

    The 11-digit format is 55910034679. 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
    5-3-255910-346-795-4-255910-0346-79