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  5. NDC Package Code: 43473-048-01 Burn

NDC Package 43473-048-01 Burn

Lidocaine Hydrochloride Gel 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:
43473-048-01
Package Description:
.9 g in 1 POUCH
Product Code:
43473-048
Proprietary Name:
Burn
Non-Proprietary Name:
Lidocaine Hydrochloride
Substance Name:
Lidocaine Hydrochloride
Usage Information:
For adults and children 2 years and older: apply to affected area not more than 4 times daily.Children under 2 years old: do not use, consult a doctor.
11-Digit NDC Billing Format:
43473004801
NDC to RxNorm Crosswalk:
  • RxCUI: 1011852 - lidocaine HCl 2 % Topical Gel
  • RxCUI: 1011852 - lidocaine hydrochloride 0.02 MG/MG Topical Gel
  • RxCUI: 1011852 - lidocaine hydrochloride 2 % Topical Jelly
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Nantong Health & Beyond Hygienic Products Inc.
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    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):
  • LIDOCAINE HYDROCHLORIDE 20 mg/g
    • Pharmacologic Class(es):
  • Amide Local Anesthetic - [EPC] (Established Pharmacologic Class)
  • Amides - [CS]
  • Antiarrhythmic - [EPC] (Established Pharmacologic Class)
  • Local Anesthesia - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-04-2022
    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 43473-048-01?

    The NDC Packaged Code 43473-048-01 is assigned to a package of .9 g in 1 pouch of Burn, a human over the counter drug labeled by Nantong Health & Beyond Hygienic Products Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 43473-048 included in the NDC Directory?

    Yes, Burn with product code 43473-048 is active and included in the NDC Directory. The product was first marketed by Nantong Health & Beyond Hygienic Products Inc. on November 04, 2022 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 43473-048-01?

    The 11-digit format is 43473004801. 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
    5-3-243473-048-015-4-243473-0048-01