NDC Package 59088-308-03 Lidotral Five Percent With Menthol

Lidocaine Hydrochloride,Menthol Liquid 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:
59088-308-03
Package Description:
30 mL in 1 BOTTLE, SPRAY
Product Code:
Proprietary Name:
Lidotral Five Percent With Menthol
Non-Proprietary Name:
Lidocaine Hydrochloride, Menthol
Substance Name:
Lidocaine Hydrochloride; Menthol
Usage Information:
For the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritation. This formulation can be used to assist patients in the treatment of mild to moderate acute or chronic aches or pain. Muscle or joint pain can be due to musculoligamentous strains, simple backache, tendonitis, osteoarthritis, rheumatoid arthritis, peripheral neuropathies such as diabetic neuropathy or post herpetic neuralgia, and other complex regional pains. If consulted by your physician, it may be used for other conditions as well. If consulted by your physician, it may be used for other conditions as well.
11-Digit NDC Billing Format:
59088030803
NDC to RxNorm Crosswalk:
  • RxCUI: 2667468 - lidocaine HCl 5 % / menthol 3 % Topical Spray
  • RxCUI: 2667468 - lidocaine hydrochloride 50 MG/ML / menthol 30 MG/ML Topical Spray
Product Type:
Human Prescription Drug
Labeler Name:
Puretek Corporation
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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.
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:
10-06-2023
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.

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Frequently Asked Questions

What is NDC 59088-308-03?

The NDC Packaged Code 59088-308-03 is assigned to a package of 30 ml in 1 bottle, spray of Lidotral Five Percent With Menthol, a human prescription drug labeled by Puretek Corporation. The product's dosage form is liquid and is administered via topical form.

Is NDC 59088-308 included in the NDC Directory?

Yes, Lidotral Five Percent With Menthol with product code 59088-308 is active and included in the NDC Directory. The product was first marketed by Puretek Corporation on October 06, 2023 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 59088-308-03?

The 11-digit format is 59088030803. 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
5-3-259088-308-035-4-259088-0308-03