Diclolidol Kit
NDC Package 59088-806-00

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Diclolidol Kit (lidocaine hcl, diclofenac sodium) kits is for the temporary relief of arthritis pain ONLY in the following areas:hand, wrist, elbow (upper body areas)foot, ankle, knee (lower body areas)this product may take up to 7 days to work for arthritis pain; it is not for immediate relief. This formulation utilizes a kit delivery system. Marketed by Puretek Corporation, this product is identified by NDC 59088-806.

Identification & Billing

NDC Package Code
59088-806-00
Package Description
1 KIT in 1 KIT * 85 g in 1 BOTTLE, WITH APPLICATOR (59088-327-07) * 1 TUBE in 1 CARTON (43598-977-10) / 100 g in 1 TUBE
Product Code
59088-806
11-Digit Billing Format
59088080600
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Diclolidol Kit
Non-Proprietary Name
Lidocaine Hcl, Diclofenac Sodium
Dosage Form
Kit - A packaged collection of related material.
Usage Information
For the temporary relief of arthritis pain ONLY in the following areas:hand, wrist, elbow (upper body areas)foot, ankle, knee (lower body areas)this product may take up to 7 days to work for arthritis pain; it is not for immediate relief. If no pain relief in 7 days, stop use. For the temporary relief of pain.

Regulatory & Marketing

Labeler Name
Puretek Corporation
Product Type
Human Prescription Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
09-09-2025
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 59088-806-00 identifies a specific commercial package of 1 kit in 1 kit * 85 g in 1 bottle, with applicator (59088-327-07) * 1 tube in 1 carton (43598-977-10) / 100 g in 1 tube of Diclolidol Kit, a human prescription drug labeled by Puretek Corporation. This kit is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Puretek Corporation on September 09, 2025. The current certification is valid through December 31, 2026.

How is this Puretek Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 59088080600. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
59088-806-00
11-Digit CMS (5-4-2)
59088-0806-00

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.