Sunburnt Plus Gel
NDC Package 68229-600-01

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 approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Sunburnt Plus (lidocaine hydrochloride) gel is clean skin and apply to affected areaadults and children 2 years of age and older: apply to affected area not more than 3-4 times dailychildren under 2 years of age: ask a doctor. This formulation utilizes a gel delivery system. Marketed by Quest Products, Llc., this product is identified by NDC 68229-600 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
68229-600-01
Package Description
1 TUBE in 1 CARTON / 118.294 mL in 1 TUBE (68229-600-02)
Product Code
68229-600
11-Digit Billing Format
68229060001
Billing Unit
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sunburnt Plus
Non-Proprietary Name
Lidocaine Hydrochloride
Substance Name
Lidocaine Hydrochloride
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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 4 g/100mL
Pharmacologic Class
Usage Information
Clean skin and apply to affected areaadults and children 2 years of age and older: apply to affected area not more than 3-4 times dailychildren under 2 years of age: ask a doctor

Regulatory & Marketing

Labeler Name
Quest Products, Llc.
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-01-2020
End Marketing Date
07-31-2026
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 68229-600-01 identifies a specific commercial package of 1 tube in 1 carton / 118.294 ml in 1 tube (68229-600-02) of Sunburnt Plus, a human over the counter drug labeled by Quest Products, Llc.. This gel 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 Quest Products, Llc. on July 01, 2020.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 68229060001. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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)
68229-600-01
11-Digit CMS (5-4-2)
68229-0600-01

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