Body Glove Sunscreen Spf 30 Liquid
NDC Package 85763-614-00

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

Package Information

Body Glove Sunscreen Spf 30 (zinc oxide, titanium dioxide) liquids is shake well and apply liberally 15 minutes before sun exposure.Hold 4-6 inches away from the skin to apply. This formulation utilizes a liquid delivery system. Marketed by Scubascreen Llc, this product is identified by NDC 85763-614 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
85763-614-00
Package Description
148 mL in 1 CAN
Product Code
85763-614
11-Digit Billing Format
85763061400

Clinical Specifications

Proprietary Name
Body Glove Sunscreen Spf 30
Non-Proprietary Name
Zinc Oxide, Titanium Dioxide
Substance Name
Titanium Dioxide; Zinc Oxide
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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)
Pharmacologic Class
Usage Information
Shake well and apply liberally 15 minutes before sun exposure.Hold 4-6 inches away from the skin to apply. Rub in.Do not spray directly into face. Spray on hands and apply to face. Avoid breathing mist.Use in well-ventilated area.Reapply:After 80 minutes of swimming or sweatingImmediately after towel dryingAt least every 2 hours.Children under 6-months of age: Ask a doctor.Sun Protection Measures:Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease the risk, regularly use a sunscreen with Broad Spectrum SPF of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10 am. - 2 pm. Wear long-sleeved shirts, pants, hats, and sunglasses.

Regulatory & Marketing

Labeler Name
Scubascreen Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-15-2025
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 85763-614-00 identifies a specific commercial package of 148 ml in 1 can of Body Glove Sunscreen Spf 30, a human over the counter drug labeled by Scubascreen Llc. This liquid is formulated for topical use and contains titanium dioxide; zinc oxide 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 Scubascreen Llc on May 15, 2025. The current certification is valid through December 31, 2026.

How is this Scubascreen Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85763061400. 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)
85763-614-00
11-Digit CMS (5-4-2)
85763-0614-00

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