Foundation Medium Spectrum Liquid
NDC Package 84958-002-01

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

Package Information

Foundation Medium Spectrum (octyl methoxycinnamate, zinc oxide, titanium dioxide) liquids is helps prevent sunbumif used as directed with other sunprotection measures (see Directions)decreases the risk of skin cancer andearly skin aging caused by the sun. This formulation utilizes a liquid delivery system. Marketed by Guangzhou Bo Win Trade Co., Ltd., this product is identified by NDC 84958-002 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
84958-002-01
Package Description
1 BOTTLE in 1 BOX / 30 g in 1 BOTTLE
Product Code
84958-002
11-Digit Billing Format
84958000201

Clinical Specifications

Proprietary Name
Foundation Medium Spectrum
Non-Proprietary Name
Octyl Methoxycinnamate, Zinc Oxide, Titanium Dioxide
Substance Name
Octinoxate; Titanium Dioxide; Zinc Oxide
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
Helps prevent sunbumif used as directed with other sunprotection measures (see Directions)decreases the risk of skin cancer andearly skin aging caused by the sun

Regulatory & Marketing

Labeler Name
Guangzhou Bo Win Trade Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-19-2024
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 84958-002-01 identifies a specific commercial package of 1 bottle in 1 box / 30 g in 1 bottle of Foundation Medium Spectrum, a human over the counter drug labeled by Guangzhou Bo Win Trade Co., Ltd.. This liquid is formulated for topical use and contains octinoxate; titanium dioxide; 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 Guangzhou Bo Win Trade Co., Ltd. on November 19, 2024. The current certification is valid through December 31, 2026.

How is this Guangzhou Bo Win Trade Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84958000201. 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)
84958-002-01
11-Digit CMS (5-4-2)
84958-0002-01

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