Pixi Sun Mist Spf 30
NDC Package 70686-101-13

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

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Pixi Sun Mist Spf 30 is sHAKE WELL BEFORE USE.APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.REAPPLY:    AFTER 40 MINUTES OF SWIMMING OR SWEATING    IMMEDIATELY AFTER TOWEL DRYING    AT LEAST EVERY 2 HOURS.SUN PROTECTION MEASURES. Marketed by Pixi, Inc, this product is identified by NDC 70686-101 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
70686-101-13
Package Description
80 mL in 1 BOTTLE, SPRAY
Product Code
70686-101
11-Digit Billing Format
70686010113

Clinical Specifications

Proprietary Name
Pixi Sun Mist Spf 30
Dosage Form
-
Usage Information
SHAKE WELL BEFORE USE.APPLY LIBERALLY 15 MINUTES BEFORE SUN EXPOSURE.REAPPLY:    AFTER 40 MINUTES OF SWIMMING OR SWEATING    IMMEDIATELY AFTER TOWEL DRYING    AT LEAST EVERY 2 HOURS.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 OF 15 OR HIGHER AND OTHER SUN PROTECTION MEASURES INCLUDING:   LIMIT TIME IN THE SUN, ESPECIALLY FROM 10 AM - 2 PM   WEAR LONG-SLEEVE SHIRTS, PANTS, HATS, AND SUNGLASSESCHILDREN UNDER 6 MONTHS. ASK A DOCTOR.

Regulatory & Marketing

Labeler Name
Pixi, Inc
FDA Application #
part352
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
08-03-2016
Listing Expiration
12-31-2019
Exclude Flag
I
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 70686-101-13 identifies a specific commercial package of 80 ml in 1 bottle, spray of Pixi Sun Mist Spf 30, labeled by Pixi, Inc. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Pixi, Inc on August 03, 2016. The current certification is valid through December 31, 2019.

How is this Pixi, Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 70686010113. 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)
70686-101-13
11-Digit CMS (5-4-2)
70686-0101-13

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