1. Home
  2. Labeler Index
  3. Meijer, Inc.
  4. 79481-0118
  5. NDC Package Code: 79481-0118-9 Oral Anesthetic Liquid

NDC Package 79481-0118-9 Oral Anesthetic Liquid

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:
79481-0118-9
Package Description:
1 BOTTLE in 1 CARTON / 14.7 g in 1 BOTTLE
Product Code:
79481-0118
Proprietary Name:
Oral Anesthetic Liquid
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
Adults and children 2 years of age and older: wipe liquid on with cotton, or cotton swab, or fingertip, apply to the affected area up to 4 times daily or as directed by a doctor/dentistchildren under 12 years of age: adult supervision should be given in the use of this productchildren under 2 years of age: do not usefor denture irritation apply a thin layer to the affected area; do not reinsert dental work until irritation/pain is relieved; rinse mouth well after reinserting
11-Digit NDC Billing Format:
79481011809
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:
    Meijer, Inc.
    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/100g
    • 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:
    02-05-2024
    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 79481-0118-9?

    The NDC Packaged Code 79481-0118-9 is assigned to a package of 1 bottle in 1 carton / 14.7 g in 1 bottle of Oral Anesthetic Liquid, a human over the counter drug labeled by Meijer, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 79481-0118 included in the NDC Directory?

    Yes, Oral Anesthetic Liquid with product code 79481-0118 is active and included in the NDC Directory. The product was first marketed by Meijer, Inc. on February 05, 2024 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 79481-0118-9?

    The 11-digit format is 79481011809. 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
    5-4-179481-0118-95-4-279481-0118-09