Sun Glazed Spf 30 Sunscreen Glow Oil
NDC Package 70157-034-01

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

Package Information

Sun Glazed Spf 30 Sunscreen Glow Oil (avobenzone, homosalate, octocrylene) oils is stop use and ask a doctor if rash occurs. This formulation utilizes a oil delivery system. Marketed by Baxter Laboratories Pty. Ltd., this product is identified by NDC 70157-034 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
70157-034-01
Package Description
150 mL in 1 BOTTLE, PLASTIC
Product Code
70157-034
11-Digit Billing Format
70157003401

Clinical Specifications

Proprietary Name
Sun Glazed Spf 30 Sunscreen Glow Oil
Non-Proprietary Name
Avobenzone, Homosalate, Octocrylene
Substance Name
Avobenzone; Homosalate; Octocrylene
Dosage Form
Oil - An unctuous, combustible substance which is liquid, or easily liquefiable, on warming, and is soluble in ether but insoluble in water. Such substances, depending on their origin, are classified as animal, mineral, or vegetable oils.
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
Stop use and ask a doctor if rash occurs.

Regulatory & Marketing

Labeler Name
Baxter Laboratories Pty. Ltd.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
09-30-2024
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 70157-034-01 identifies a specific commercial package of 150 ml in 1 bottle, plastic of Sun Glazed Spf 30 Sunscreen Glow Oil, a human over the counter drug labeled by Baxter Laboratories Pty. Ltd.. This oil is formulated for topical use and contains avobenzone; homosalate; 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 Baxter Laboratories Pty. Ltd. on September 30, 2024. The current certification is valid through December 31, 2026.

How is this Baxter Laboratories Pty. Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70157003401. 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)
70157-034-01
11-Digit CMS (5-4-2)
70157-0034-01

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