Sulisrx Sunburn Relief Kit
NDC Package 87735-003-01

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

Package Information

Sulisrx Sunburn Relief Kit (sunburn relief kit) kits is pain reliever & antihistamine PurposeExternal Analgesic. This formulation utilizes a kit delivery system. Marketed by Sephoris Pharmaceuticals, Llc, this product is identified by NDC 87735-003.

Identification & Billing

NDC Package Code
87735-003-01
Package Description
1 KIT in 1 KIT * 59 mL in 1 BOTTLE, SPRAY (87735-001-01) * 1 TABLET, FILM COATED in 1 BOTTLE (87735-002-01)
Product Code
87735-003
11-Digit Billing Format
87735000301

Clinical Specifications

Proprietary Name
Sulisrx Sunburn Relief Kit
Non-Proprietary Name
Sunburn Relief Kit
Dosage Form
Kit - A packaged collection of related material.
Usage Information
Pain reliever & antihistamine PurposeExternal Analgesic

Regulatory & Marketing

Labeler Name
Sephoris Pharmaceuticals, Llc
Product Type
Human Otc 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
09-03-2026
Listing Expiration
12-31-2027
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 87735-003-01 identifies a specific commercial package of 1 kit in 1 kit * 59 ml in 1 bottle, spray (87735-001-01) * 1 tablet, film coated in 1 bottle (87735-002-01) of Sulisrx Sunburn Relief Kit, a human over the counter drug labeled by Sephoris Pharmaceuticals, Llc. 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 Sephoris Pharmaceuticals, Llc on September 03, 2026. The current certification is valid through December 31, 2027.

How is this Sephoris Pharmaceuticals, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87735000301. 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)
87735-003-01
11-Digit CMS (5-4-2)
87735-0003-01

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