Numb Skin
NDC Package 70907-002-50

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Numb Skin is use NumbSkin® Topical Anesthetic Foam Soap to cleanse the targeted area. Marketed by Seenext Venture Ltd, this product is identified by NDC 70907-002 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
70907-002-50
Package Description
1 TUBE in 1 CARTRIDGE / 50 g in 1 TUBE
Product Code
70907-002
11-Digit Billing Format
70907000250

Clinical Specifications

Proprietary Name
Numb Skin
Dosage Form
-
Usage Information
Use NumbSkin® Topical Anesthetic Foam Soap to cleanse the targeted area. Shake well before each use.Apply 2 to 3 pumps of foam soap andgently rub into the skin. Leave it onfor 5 to 10 minutes. Rinse off gentlywith running water or wipe with cleanpaper towel.Use before, during andafter the procedure.Make sure tocover the bottle tightly when not inuse, otherwise, the anesthetic effect will be lessened.Adults and children two years old and older: Use to clean minor cuts, scrapes, and burns by thoroughly washing with water. Rinse and air dry. Use no more than three times daily. Children under two years of age, ask a doctor.

Regulatory & Marketing

Labeler Name
Seenext Venture Ltd
FDA Application #
part348
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
09-11-2017
Listing Expiration
12-31-2023
Exclude Flag
I
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 70907-002-50 identifies a specific commercial package of 1 tube in 1 cartridge / 50 g in 1 tube of Numb Skin, labeled by Seenext Venture Ltd. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Seenext Venture Ltd on September 11, 2017. The current certification is valid through December 31, 2023.

How is this Seenext Venture Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70907000250. 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)
70907-002-50
11-Digit CMS (5-4-2)
70907-0002-50

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