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  5. NDC Package Code: 85763-614-00 Body Glove Sunscreen Spf 30

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

Zinc Oxide,Titanium Dioxide Liquid Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
85763-614-00
Package Description:
148 mL in 1 CAN
Product Code:
85763-614
Proprietary Name:
Body Glove Sunscreen Spf 30
Non-Proprietary Name:
Zinc Oxide, Titanium Dioxide
Substance Name:
Titanium Dioxide; Zinc Oxide
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.
11-Digit NDC Billing Format:
85763061400
Product Type:
Human Otc Drug
Labeler Name:
Scubascreen Llc
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(s):
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(es):
Sample Package:
No
FDA Application Number:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-15-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code 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 disclaimer below.

Frequently Asked Questions

What is NDC 85763-614-00?

The NDC Packaged Code 85763-614-00 is assigned to a package of 148 ml in 1 can of Body Glove Sunscreen Spf 30, a human over the counter drug labeled by Scubascreen Llc. The product's dosage form is liquid and is administered via topical form.

Is NDC 85763-614 included in the NDC Directory?

Yes, Body Glove Sunscreen Spf 30 with product code 85763-614 is active and included in the NDC Directory. The product was first marketed by Scubascreen Llc on May 15, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 85763-614-00?

The 11-digit format is 85763061400. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-285763-614-005-4-285763-0614-00