Somxl Homeopathic Wart Remover Cream
NDC Package 70463-725-01

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

Package Information

Somxl Homeopathic Wart Remover (thuja occidentalis leafy twig) cream is •Wash affected area (May soak wart in warm water for 15-minutes if desired). This formulation utilizes a cream delivery system. Marketed by Wr Group Skin Care Ltd, this product is identified by NDC 70463-725.

Identification & Billing

NDC Package Code
70463-725-01
Package Description
1 TUBE in 1 BOX / 15 g in 1 TUBE
Product Code
70463-725
11-Digit Billing Format
70463072501

Clinical Specifications

Proprietary Name
Somxl Homeopathic Wart Remover
Non-Proprietary Name
Thuja Occidentalis Leafy Twig
Substance Name
Thuja Occidentalis Leafy Twig
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
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)
THUJA OCCIDENTALIS LEAFY TWIG 6 [hp_X]/15g
Usage Information
•Wash affected area (May soak wart in warm water for 15-minutes if desired). • Dry area throughly. • Apply small amount with applicator to cover each wart. Let dry.  • Repeat this procedure once or twice daily as needed for up to 12-weeks.

Regulatory & Marketing

Labeler Name
Wr Group Skin Care Ltd
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
02-05-2016
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 70463-725-01 identifies a specific commercial package of 1 tube in 1 box / 15 g in 1 tube of Somxl Homeopathic Wart Remover, a human over the counter drug labeled by Wr Group Skin Care Ltd. This cream is formulated for topical use and contains thuja occidentalis leafy twig 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 Wr Group Skin Care Ltd on February 05, 2016. The current certification is valid through December 31, 2026.

How is this Wr Group Skin Care Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70463072501. 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)
70463-725-01
11-Digit CMS (5-4-2)
70463-0725-01

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