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  5. NDC Package Code: 69876-1740-0 Neuroflex Topical Pain Relieving Liquid

NDC Package 69876-1740-0 Neuroflex Topical Pain Relieving Liquid

Camphor (synthetic),Menthol Solution Topical - 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:
69876-1740-0
Package Description:
118 mL in 1 BOTTLE, SPRAY
Product Code:
69876-1740
Proprietary Name:
Neuroflex Topical Pain Relieving Liquid
Non-Proprietary Name:
Camphor (synthetic), Menthol
Substance Name:
Camphor (synthetic); Menthol
Usage Information:
• Adults and children 2 years of age and older. Apply to affected areas not more than 3 to 4 times daily. No need to rub in. • Children under 2 years of age: Consult a physician.
11-Digit NDC Billing Format:
69876174000
NDC to RxNorm Crosswalk:
  • RxCUI: 2534165 - camphor 3 % / menthol 2 % Topical Solution
  • RxCUI: 2534165 - camphor 30 MG/ML / menthol 20 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Almark Products Inc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • CAMPHOR (SYNTHETIC) 30 mg/mL
  • MENTHOL 20 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-01-2021
    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 69876-1740-0?

    The NDC Packaged Code 69876-1740-0 is assigned to a package of 118 ml in 1 bottle, spray of Neuroflex Topical Pain Relieving Liquid, a human over the counter drug labeled by Almark Products Inc. The product's dosage form is solution and is administered via topical form.

    Is NDC 69876-1740 included in the NDC Directory?

    Yes, Neuroflex Topical Pain Relieving Liquid with product code 69876-1740 is active and included in the NDC Directory. The product was first marketed by Almark Products Inc on April 01, 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 69876-1740-0?

    The 11-digit format is 69876174000. 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
    5-4-169876-1740-05-4-269876-1740-00