Stout Daily Spf For Men Liquid
NDC Package 71100-001-90

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

Package Information

Stout Daily Spf For Men (sunscreen) liquids is a medication used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). This formulation utilizes a liquid delivery system. Marketed by Stout Face Care Inc., this product is identified by NDC 71100-001 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
71100-001-90
Package Description
90 mL in 1 TUBE
Product Code
71100-001
11-Digit Billing Format
71100000190

Clinical Specifications

Proprietary Name
Stout Daily Spf For Men
Non-Proprietary Name
Sunscreen
Substance Name
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)
ZINC OXIDE 8.82 g/90mL
Usage Information
This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.

Regulatory & Marketing

Labeler Name
Stout Face Care Inc.
Product Type
Human Otc Drug
FDA Application #
part352
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
03-01-2017
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 71100-001-90 identifies a specific commercial package of 90 ml in 1 tube of Stout Daily Spf For Men, a human over the counter drug labeled by Stout Face Care Inc.. This liquid is formulated for topical use and contains 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 Stout Face Care Inc. on March 01, 2017. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

This medication is used to treat and prevent diaper rash and other minor skin irritations (e.g., burns, cuts, scrapes). It works by forming a barrier on the skin to protect it from irritants/moisture.

How is this Stout Face Care Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71100000190. 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)
71100-001-90
11-Digit CMS (5-4-2)
71100-0001-90

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