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  5. NDC Package Code: 59088-304-03 Lidotral Two Percent

NDC Package 59088-304-03 Lidotral Two Percent

Lidocaine Hydrochloride Spray 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:
59088-304-03
Package Description:
30 mL in 1 BOTTLE, SPRAY
Product Code:
59088-304
Proprietary Name:
Lidotral Two Percent
Non-Proprietary Name:
Lidocaine Hydrochloride
Substance Name:
Lidocaine Hydrochloride
Usage Information:
For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritation.
11-Digit NDC Billing Format:
59088030403
NDC to RxNorm Crosswalk:
  • RxCUI: 1010769 - lidocaine HCl 2 % Topical Spray
  • RxCUI: 1010769 - lidocaine hydrochloride 20 MG/ML Topical Spray
  • RxCUI: 1010769 - lidocaine hydrochloride 2 % Topical Spray
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Puretek Corporation
    Dosage Form:
    Spray - A liquid minutely divided as by a jet of air or steam.
    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/mL
    • 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
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    05-14-2024
    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 59088-304-03?

    The NDC Packaged Code 59088-304-03 is assigned to a package of 30 ml in 1 bottle, spray of Lidotral Two Percent, a human prescription drug labeled by Puretek Corporation. The product's dosage form is spray and is administered via topical form.

    Is NDC 59088-304 included in the NDC Directory?

    Yes, Lidotral Two Percent with product code 59088-304 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on May 14, 2024 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 59088-304-03?

    The 11-digit format is 59088030403. 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
    5-3-259088-304-035-4-259088-0304-03