Electrum Numb Foam Soap
NDC Package 76348-596-17

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

Package Information

Electrum Numb Foam (lidocaine hci) soaps Can be used instead of soap and water to help clean minor cuts, scrapes, and burns.For the temporary relief of discomfort and pain associated with dermal procedures such as tattoo removal, tattoo, dermarolling, electrolysis, microblading and piercing.Temporarily relieves pain and itch while helping prevent infectionDirectionsShake Well before each use. This formulation utilizes a soap delivery system. Marketed by Renu Laboratories, Llc, this product is identified by NDC 76348-596 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
76348-596-17
Package Description
48 mL in 1 BOTTLE, PUMP
Product Code
76348-596
11-Digit Billing Format
76348059617
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Electrum Numb Foam
Non-Proprietary Name
Lidocaine Hci
Substance Name
Lidocaine Hydrochloride
Dosage Form
Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
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)
LIDOCAINE HYDROCHLORIDE 1.92 g/48mL
Pharmacologic Class
Usage Information
Can be used instead of soap and water to help clean minor cuts, scrapes, and burns.For the temporary relief of discomfort and pain associated with dermal procedures such as tattoo removal, tattoo, dermarolling, electrolysis, microblading and piercing.Temporarily relieves pain and itch while helping prevent infectionDirectionsShake Well before each use. Apply 2 to 3 pumps of foam soap and gently rub into skin. Leave it on for 5 to 10 minutes. Rinse off gently with running water or wipe with a clean paper towel. Use before, during and after the procedure. Keep bottle tightened to keep product fresh and effective. Adults and children 2 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 3 times a day. Children under two years of age, ask a doctorThis product is used as . PurposeTopical anestheticFirst aid antiseptic

Regulatory & Marketing

Labeler Name
Renu Laboratories, Llc
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-29-2021
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 76348-596-17 identifies a specific commercial package of 48 ml in 1 bottle, pump of Electrum Numb Foam, a human over the counter drug labeled by Renu Laboratories, Llc. This soap is formulated for topical use and contains lidocaine hydrochloride 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 Renu Laboratories, Llc on July 29, 2021. The current certification is valid through December 31, 2026.

How is this Renu Laboratories, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 76348059617. 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)
76348-596-17
11-Digit CMS (5-4-2)
76348-0596-17

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