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  5. NDC Package Code: 58593-782-02 Finafta Multioral

NDC Package 58593-782-02 Finafta Multioral

Benzocaine Spray 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:
58593-782-02
Package Description:
1 BOTTLE, SPRAY in 1 CARTON / 59 mL in 1 BOTTLE, SPRAY
Product Code:
58593-782
Proprietary Name:
Finafta Multioral
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
USESFor the temporary relief of occasional minor irritation, pain, sore mouth, pain associated with canker sores or pain due to minor irritation of the mouth and gums cause by dentures or othodontic applicances.
11-Digit NDC Billing Format:
58593078202
NDC to RxNorm Crosswalk:
  • RxCUI: 1110816 - benzocaine 7.5 % Mucosal Spray
  • RxCUI: 1110816 - benzocaine 75 MG/ML Mucosal Spray
  • RxCUI: 1110820 - Finafta Multi Oral 7.5 % Mucosal Spray
  • RxCUI: 1110820 - benzocaine 75 MG/ML Mucosal Spray [Finafta Multi Oral]
  • RxCUI: 1110820 - Finafta Multi Oral 75 MG/ML Mucosal Spray
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Efficient Laboratories Inc.
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • BENZOCAINE 7.5 mg/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:
    part356
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    09-01-2004
    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 58593-782-02?

    The NDC Packaged Code 58593-782-02 is assigned to a package of 1 bottle, spray in 1 carton / 59 ml in 1 bottle, spray of Finafta Multioral, a human over the counter drug labeled by Efficient Laboratories Inc.. The product's dosage form is spray and is administered via oral form.

    Is NDC 58593-782 included in the NDC Directory?

    Yes, Finafta Multioral with product code 58593-782 is active and included in the NDC Directory. The product was first marketed by Efficient Laboratories Inc. on September 01, 2004 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 58593-782-02?

    The 11-digit format is 58593078202. 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
    5-3-258593-782-025-4-258593-0782-02