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  5. NDC Package Code: 36800-382-03 Benzethonium Chloride Plus Dyclonine Hydrochloride

NDC Package 36800-382-03 Benzethonium Chloride Plus Dyclonine Hydrochloride

Liquid Bandage Liquid 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:
36800-382-03
Package Description:
9 mL in 1 BOTTLE, WITH APPLICATOR
Product Code:
36800-382
Proprietary Name:
Benzethonium Chloride Plus Dyclonine Hydrochloride
Non-Proprietary Name:
Liquid Bandage
Substance Name:
Benzethonium Chloride; Dyclonine Hydrochloride
Usage Information:
Clean affected areaapply a small amount on the area 1-3 times dailylet drya second coating may be applied for extra protectionto remove, apply more Liquid Bandage and quickly wipe offfinger nail polish remover may dissolve Liquid Bandage
11-Digit NDC Billing Format:
36800038203
Product Type:
Human Otc Drug
Labeler Name:
Topco Associates Llc
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):
  • 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):
  • BENZETHONIUM CHLORIDE .2 mg/9mL
  • DYCLONINE HYDROCHLORIDE .75 mg/9mL
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    07-10-2014
    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 36800-382-03?

    The NDC Packaged Code 36800-382-03 is assigned to a package of 9 ml in 1 bottle, with applicator of Benzethonium Chloride Plus Dyclonine Hydrochloride, a human over the counter drug labeled by Topco Associates Llc. The product's dosage form is liquid and is administered via topical form.

    Is NDC 36800-382 included in the NDC Directory?

    Yes, Benzethonium Chloride Plus Dyclonine Hydrochloride with product code 36800-382 is active and included in the NDC Directory. The product was first marketed by Topco Associates Llc on July 10, 2014 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 36800-382-03?

    The 11-digit format is 36800038203. 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
    5-3-236800-382-035-4-236800-0382-03