Mineral Based Foam Sunscreen Tinted Aerosol, Foam
NDC Package 81679-210-04

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

Package Information

Mineral Based Foam Sunscreen Tinted (titanium dioxide, zinc oxide) aerosols is a human otc drug administered via topical route. This formulation utilizes a aerosol, foam delivery system. Marketed by Kathleen P. Hutton, M.d., Inc. A Professional Corporation, this product is identified by NDC 81679-210 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
81679-210-04
Package Description
100 g in 1 BOTTLE, DISPENSING
Product Code
81679-210
11-Digit Billing Format
81679021004

Clinical Specifications

Proprietary Name
Mineral Based Foam Sunscreen Tinted
Non-Proprietary Name
Titanium Dioxide, Zinc Oxide
Substance Name
Titanium Dioxide; Zinc Oxide
Dosage Form
Aerosol, Foam - A dosage form containing one or more active ingredients, surfactants, aqueous or nonaqueous liquids, and the propellants; if the propellant is in the internal (discontinuous) phase (i.e., of the oil-in-water type), a stable foam is discharged, and if the propellant is in the external (continuous) phase (i.e., of the water-in-oil type), a spray or a quick-breaking foam is discharged.
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)

Regulatory & Marketing

Labeler Name
Kathleen P. Hutton, M.d., Inc. A Professional Corporation
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-10-2021
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 81679-210-04 identifies a specific commercial package of 100 g in 1 bottle, dispensing of Mineral Based Foam Sunscreen Tinted, a human over the counter drug labeled by Kathleen P. Hutton, M.d., Inc. A Professional Corporation. This aerosol, foam is formulated for topical use and contains 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 Kathleen P. Hutton, M.d., Inc. A Professional Corporation on June 10, 2021. The current certification is valid through December 31, 2026.

How is this Kathleen P. Hutton, M.d., Inc. A Professional Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 81679021004. 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)
81679-210-04
11-Digit CMS (5-4-2)
81679-0210-04

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