Fitish Spf 50 Face Stick
NDC Package 84417-002-01

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

Package Information

Fitish Spf 50 Face sticks is apply directly to clean skin 15 minutes before sun exposure and anywhere you want extra glow. This formulation utilizes a stick delivery system. Marketed by Fitish Holdings, Llc, this product is identified by NDC 84417-002.

Identification & Billing

NDC Package Code
84417-002-01
Package Description
50 g in 1 BOTTLE
Product Code
84417-002
11-Digit Billing Format
84417000201

Clinical Specifications

Proprietary Name
Fitish Spf 50 Face
Non-Proprietary Name
Fitish Spf 50 Face
Substance Name
Octinoxate; Octocrylene; Octisalate
Dosage Form
Stick - A dosage form prepared in a relatively long and slender often cylindrical form.
Administration Route
Cutaneous - Administration to the skin.
Active Ingredient(s)
Usage Information
Apply directly to clean skin 15 minutes before sun exposure and anywhere you want extra glow. Reapply after40 minutes of swimming or sweating, immediately after towel drying and at least every 2 hours. Can be usedon body as well.Sun Protection Measures Spending time in the sun increases your risk of skin cancer and early skin aging.To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and othersun protection measures including limiting time in the sun, especially from 10 a.m.-2 p.m. and wear long-sleevedshirts, pants, hats and sunglasses

Regulatory & Marketing

Labeler Name
Fitish Holdings, Llc
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
06-26-2024
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 84417-002-01 identifies a specific commercial package of 50 g in 1 bottle of Fitish Spf 50 Face, a human over the counter drug labeled by Fitish Holdings, Llc. This stick is formulated for cutaneous use and contains octinoxate; octocrylene; octisalate 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 Fitish Holdings, Llc on June 26, 2024. The current certification is valid through December 31, 2027.

How is this Fitish Holdings, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 84417000201. 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)
84417-002-01
11-Digit CMS (5-4-2)
84417-0002-01

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