NDC Package 81902-104-15 Zylotrol Maximum Pain

Lidocaine 4%,Menthol 1% Patch 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:
81902-104-15
Package Description:
15 PATCH in 1 BOX / 3 g in 1 PATCH
Product Code:
Proprietary Name:
Zylotrol Maximum Pain
Non-Proprietary Name:
Lidocaine 4%, Menthol 1%
Substance Name:
Lidocaine; Menthol
Usage Information:
Adult and children 12 years of age and over:Clean and dry affected areaRemove film from patch and apply to the skin (see illustration)Apply 1 patch at a time to affected area, not more than 3 to 4 times dailyRemove patch from the skin after at most 8-hour applicationChildren under 12 years of age: Consult a doctor
11-Digit NDC Billing Format:
81902010415
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
Product Type:
Human Otc Drug
Labeler Name:
Whitestone Products Llc
Dosage Form:
Patch - A drug delivery system that often contains an adhesive backing that is usually applied to an external site on the body. Its ingredients either passively diffuse from, or are actively transported from, some portion of the patch. Depending upon the patch, the ingredients are either delivered to the outer surface of the body or into the body. A patch is sometimes synonymous with the terms ‘extended release film’ and ‘system’.
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:
505G(a)(3)
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
12-23-2022
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 81902-104-15?

The NDC Packaged Code 81902-104-15 is assigned to a package of 15 patch in 1 box / 3 g in 1 patch of Zylotrol Maximum Pain, a human over the counter drug labeled by Whitestone Products Llc. The product's dosage form is patch and is administered via topical form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

Is NDC 81902-104 included in the NDC Directory?

Yes, Zylotrol Maximum Pain with product code 81902-104 is active and included in the NDC Directory. The product was first marketed by Whitestone Products Llc on December 23, 2022 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 NDC billing unit for package 81902-104-15?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

What is the 11-digit format for NDC 81902-104-15?

The 11-digit format is 81902010415. 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
5-3-281902-104-155-4-281902-0104-15