Zinc Oxide 20% Cream
NDC Package 87392-001-02

11-digit billing NDC: 87392000102
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Zinc Oxide 20% (sunscreen spf 30) cream is apply evenly to face and neck 15 minutes before sun exposure reapply: After 80 minutes of swimming or sweating. This formulation utilizes a cream delivery system. Marketed by Shade Rayz Llc, this product is identified by NDC 87392-001 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
87392-001-02
Package Description
50 mL in 1 BOTTLE
Product Code
87392-001
11-Digit Billing Format
87392000102

Clinical Specifications

Proprietary Name
Zinc Oxide 20%
Non-Proprietary Name
Sunscreen Spf 30
Substance Name
Zinc Oxide
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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)
ZINC OXIDE 20 g/100mL
Pharmacologic Class
Usage Information
Apply evenly to face and neck 15 minutes before sun exposure reapply: After 80 minutes of swimming or sweating . Immediately after towel drying . At least every 2 hours • Sun ProtectionMeasures.Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including: Limit time in the sun, especially from 10a.m.– 2p.m. . Wear long-sleeve shirts, pants, hats, and sunglasses. . Children under 6 months: Ask a doctor.

Regulatory & Marketing

Labeler Name
Shade Rayz Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-09-2026
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 87392-001-02 identifies a specific commercial package of 50 ml in 1 bottle of Zinc Oxide 20%, a human over the counter drug labeled by Shade Rayz Llc. This cream is formulated for topical use and contains 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 Shade Rayz Llc on October 09, 2026. The current certification is valid through December 31, 2027.

How is this Shade Rayz Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87392000102. 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)
87392-001-02
11-Digit CMS (5-4-2)
87392-0001-02

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