Golden Glow Shimmer Mist Spray
NDC Package 81104-015-03

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

Package Information

Golden Glow Shimmer Mist (avobenzone, homosalate, octisalate, octocrylene) sprays is shake well before use.Avoid Eye Area.Use as top up sunscreen only.Hold 8-10” away from your body and spray liberally & evenly until skin feels moist 20 minutes before sun exposure.Do not apply in windy conditions.Use in well-ventilated area.Avoid inhalation.Reapply at least every 2 hours.Reapply immediately after swimming, sweating or towel drying.Use a water-resistant sunscreen if swimming or sweating.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. This formulation utilizes a spray delivery system. Marketed by Naked Sundays Pty Ltd, this product is identified by NDC 81104-015 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
81104-015-03
Package Description
75 mL in 1 BOTTLE, SPRAY
Product Code
81104-015
11-Digit Billing Format
81104001503

Clinical Specifications

Proprietary Name
Golden Glow Shimmer Mist
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.
Active Ingredient(s)
Usage Information
Shake well before use.Avoid Eye Area.Use as top up sunscreen only.Hold 8-10” away from your body and spray liberally & evenly until skin feels moist 20 minutes before sun exposure.Do not apply in windy conditions.Use in well-ventilated area.Avoid inhalation.Reapply at least every 2 hours.Reapply immediately after swimming, sweating or towel drying.Use a water-resistant sunscreen if swimming or sweating.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 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 10.00AM-2.00PMWear long-sleeved shirts, pants, hats, and sunglasses

Regulatory & Marketing

Labeler Name
Naked Sundays Pty Ltd
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
01-21-2026
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 81104-015-03 identifies a specific commercial package of 75 ml in 1 bottle, spray of Golden Glow Shimmer Mist, a human over the counter drug labeled by Naked Sundays Pty Ltd. 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 Naked Sundays Pty Ltd on January 21, 2026. The current certification is valid through December 31, 2027.

How is this Naked Sundays Pty Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81104001503. 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)
81104-015-03
11-Digit CMS (5-4-2)
81104-0015-03

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