Sugargirl Glowy Spf 30 Face Screen Sunlight Shimmer Sunscreen For The Face Liquid
NDC Package 85179-032-00

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

Package Information

Sugargirl Glowy Spf 30 Face Screen Sunlight Shimmer Sunscreen For The Face (homosalate, octocrylene, octisalate, octinoxate, avobenzone) liquids is apply generously and evenly 15 minutes before sun exposure.Reapply at least every 2 hoursUse a water resistant sunscreen if swimming or sweating.Children under 6 month: ask a doctor. This formulation utilizes a liquid delivery system. Marketed by I World Llc, this product is identified by NDC 85179-032 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
85179-032-00
Package Description
50 g in 1 TUBE
Product Code
85179-032
11-Digit Billing Format
85179003200

Clinical Specifications

Proprietary Name
Sugargirl Glowy Spf 30 Face Screen Sunlight Shimmer Sunscreen For The Face
Non-Proprietary Name
Homosalate, Octocrylene, Octisalate, Octinoxate, Avobenzone
Substance Name
Avobenzone; Homosalate; Octinoxate; Octisalate; Octocrylene
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)
Usage Information
Apply generously and evenly 15 minutes before sun exposure.Reapply at least every 2 hoursUse a water resistant sunscreen if swimming or sweating.Children under 6 month: ask a doctor.

Regulatory & Marketing

Labeler Name
I World Llc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
12-06-2025
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 85179-032-00 identifies a specific commercial package of 50 g in 1 tube of Sugargirl Glowy Spf 30 Face Screen Sunlight Shimmer Sunscreen For The Face, a human over the counter drug labeled by I World Llc. This liquid is formulated for topical use and contains avobenzone; homosalate; octinoxate; 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 I World Llc on December 06, 2025. The current certification is valid through December 31, 2027.

How is this I World Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 85179003200. 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)
85179-032-00
11-Digit CMS (5-4-2)
85179-0032-00

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