Spf 70 Kids Sunscreen Spray
NDC Package 72839-310-36

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Spf 70 Kids Sunscreen (avobenzone, homosalate, octisalate, octocrylene) sprays is apply liberally 15 minutes before sun exposure. This formulation utilizes a spray delivery system. Marketed by Derma Care Research Labs, Llc, this product is identified by NDC 72839-310 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
72839-310-36
Package Description
170 g in 1 CAN
Product Code
11-Digit Billing Format
72839031036

Clinical Specifications

Proprietary Name
Spf 70 Kids Sunscreen
Non-Proprietary Name
Avobenzone, Homosalate, Octisalate, Octocrylene
Substance Name
Avobenzone; Homosalate; Octisalate; Octocrylene
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.
Usage Information
Apply liberally 15 minutes before sun exposure. Reapply:after 80 minutes of swimming or sweatingimmediately after towel dryingat least every 2 hoursSun protection measures: spending time n the sun increases your risk of skin cancer and early skin aging. To decrease risk, regularly use a sunscreen with broad spectrum SPF of 15 or higher and other sun protection measure including: limit time in the sun, especially from 10 am to 2 pmwear long-sleeved shirts, pants, hats, and sunglasses.Children under 6 months: ask a doctor.Hold container 4 to 6 inches from the skin to apply. Do not spray directly into face. Spray on hands then apply to face. Do no apply in windy conditions. Use in a well-ventilated area.

Regulatory & Marketing

Labeler Name
Derma Care Research Labs, Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-23-2023
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (72839-310). Click a package code to view its specific billing and regulatory data.

170 g in 1 CAN
170 g in 1 CAN
170 g in 1 CAN

* 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 72839-310-36 identifies a specific commercial package of 170 g in 1 can of Spf 70 Kids Sunscreen, a human over the counter drug labeled by Derma Care Research Labs, Llc. This spray is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene 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 Derma Care Research Labs, Llc on May 23, 2023. The current certification is valid through December 31, 2027.

How is this Derma Care Research Labs, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72839031036. 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)
72839-310-36
11-Digit CMS (5-4-2)
72839-0310-36

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