Gurunanda Pain Relief Spray
NDC Package 70708-101-02

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

Package Information

Gurunanda Pain Relief (lidocaine hydrochloride) sprays is adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times dailyChildren under 12 years of age: Do not use. This formulation utilizes a spray delivery system. Marketed by Gurunanda, Llc., this product is identified by NDC 70708-101 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
70708-101-02
Package Description
1 BOTTLE, SPRAY in 1 CARTON / 59 mL in 1 BOTTLE, SPRAY
Product Code
70708-101
11-Digit Billing Format
70708010102
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Gurunanda Pain Relief
Non-Proprietary Name
Lidocaine Hydrochloride
Substance Name
Lidocaine Hydrochloride
Dosage Form
Spray - A liquid minutely divided as by a jet of air or steam.
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 40 mg/mL
Pharmacologic Class
Usage Information
Adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times dailyChildren under 12 years of age: Do not use. Consult a doctor

Regulatory & Marketing

Labeler Name
Gurunanda, Llc.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-01-2025
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 70708-101-02 identifies a specific commercial package of 1 bottle, spray in 1 carton / 59 ml in 1 bottle, spray of Gurunanda Pain Relief, a human over the counter drug labeled by Gurunanda, Llc.. This spray 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 Gurunanda, Llc. on July 01, 2025. The current certification is valid through December 31, 2026.

How is this Gurunanda, Llc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70708010102. 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)
70708-101-02
11-Digit CMS (5-4-2)
70708-0101-02

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