NDC Package 67234-037-01 Burnx Pain Relieving Burn

Lidocaine Hydrochloride Gel Topical - View Billable Units, 11-Digit Format, RxNorm

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:
67234-037-01
Package Description:
1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Code:
Proprietary Name:
Burnx Pain Relieving Burn
Non-Proprietary Name:
Lidocaine Hydrochloride
Substance Name:
Lidocaine Hydrochloride
Usage Information:
Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times dailyChildren under 2 years of age: Consult a doctor
11-Digit NDC Billing Format:
67234003701
NDC to RxNorm Crosswalk:
  • RxCUI: 1009433 - lidocaine HCl 2.5 % Topical Gel
  • RxCUI: 1009433 - lidocaine hydrochloride 0.025 MG/MG Topical Gel
  • RxCUI: 1009433 - lidocaine hydrochloride 2.5 % Topical Gel
  • RxCUI: 1862084 - BurnX 2.5 % Topical Gel
  • RxCUI: 1862084 - lidocaine hydrochloride 0.025 MG/MG Topical Gel [BurnX]
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Natureplex, Llc
    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):
    Sample Package:
    No
    FDA Application Number:
    part348
    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:
    04-10-2010
    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 67234-037-01?

    The NDC Packaged Code 67234-037-01 is assigned to a package of 1 tube in 1 carton / 28 g in 1 tube of Burnx Pain Relieving Burn, a human over the counter drug labeled by Natureplex, Llc. The product's dosage form is gel and is administered via topical form.

    Is NDC 67234-037 included in the NDC Directory?

    Yes, Burnx Pain Relieving Burn with product code 67234-037 is active and included in the NDC Directory. The product was first marketed by Natureplex, Llc on April 10, 2010 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 67234-037-01?

    The 11-digit format is 67234003701. 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
    5-3-267234-037-015-4-267234-0037-01