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  5. NDC Package Code: 79903-037-34 Sunburn Relief

NDC Package 79903-037-34 Sunburn Relief

Lidocaine Hcl 0.5% 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:
79903-037-34
Package Description:
226 g in 1 BOTTLE, PLASTIC
Product Code:
79903-037
Proprietary Name:
Sunburn Relief
Non-Proprietary Name:
Lidocaine Hcl 0.5%
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: ask a doctor
11-Digit NDC Billing Format:
79903003734
NDC to RxNorm Crosswalk:
  • RxCUI: 1011849 - lidocaine HCl 0.5 % Topical Gel
  • RxCUI: 1011849 - lidocaine hydrochloride 0.005 MG/MG Topical Gel
  • RxCUI: 1011849 - lidocaine hydrochloride 0.5 % Topical Gel
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Walmart 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 .5 g/100g
    • 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:
    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:
    12-23-2020
    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 79903-037-34?

    The NDC Packaged Code 79903-037-34 is assigned to a package of 226 g in 1 bottle, plastic of Sunburn Relief, a human over the counter drug labeled by Walmart Inc.. The product's dosage form is gel and is administered via topical form.

    Is NDC 79903-037 included in the NDC Directory?

    Yes, Sunburn Relief with product code 79903-037 is active and included in the NDC Directory. The product was first marketed by Walmart Inc. on December 23, 2020 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 79903-037-34?

    The 11-digit format is 79903003734. 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
    5-3-279903-037-345-4-279903-0037-34