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  5. NDC Package Code: 73288-004-01 Sting Relief Prep Pad

NDC Package 73288-004-01 Sting Relief Prep Pad

Benzocaine 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:
73288-004-01
Package Description:
2 PATCH in 1 PACKET / .4 g in 1 PATCH
Product Code:
73288-004
Proprietary Name:
Sting Relief Prep Pad
Non-Proprietary Name:
Benzocaine
Substance Name:
Benzocaine
Usage Information:
Uses: For temporary relief of pain and itching associated with minor burns, scrapes, and insect bites
11-Digit NDC Billing Format:
73288000401
NDC to RxNorm Crosswalk:
  • RxCUI: 2197238 - benzocaine 10 % Medicated Pad
  • RxCUI: 2197238 - benzocaine 100 MG/ML Medicated Pad
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Ningbo Tianbo First Aid Product Co., Ltd.
    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):
  • BENZOCAINE 10 g/100g
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M017
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-18-2019
    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 73288-004-01?

    The NDC Packaged Code 73288-004-01 is assigned to a package of 2 patch in 1 packet / .4 g in 1 patch of Sting Relief Prep Pad, a human over the counter drug labeled by Ningbo Tianbo First Aid Product Co., Ltd.. The product's dosage form is solution and is administered via topical form.

    Is NDC 73288-004 included in the NDC Directory?

    Yes, Sting Relief Prep Pad with product code 73288-004 is active and included in the NDC Directory. The product was first marketed by Ningbo Tianbo First Aid Product Co., Ltd. on August 18, 2019 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 73288-004-01?

    The 11-digit format is 73288000401. 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
    5-3-273288-004-015-4-273288-0004-01