Tula Skincare Go Away Acne Spot Treatment
NDC Package 72296-040-15

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.

Tula Skincare Go Away Acne Spot Treatment is • clean the skin thoroughly before applying this product • cover the entire affected area with a thin layer one to three times daily • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor • if bothersome dryness or peeling occurs, reduce application to once a day or every other day. Marketed by Tula Life Llc, this product is identified by NDC 72296-040 and is authorized under FDA application part333D.

Identification & Billing

NDC Package Code
72296-040-15
Package Description
1 TUBE in 1 CARTON / 15 g in 1 TUBE
Product Code
72296-040
11-Digit Billing Format
72296004015

Clinical Specifications

Proprietary Name
Tula Skincare Go Away Acne Spot Treatment
Dosage Form
-
Usage Information
• clean the skin thoroughly before applying this product • cover the entire affected area with a thin layer one to three times daily • because excessive drying of the skin may occur, start with one application daily, then gradually increase to two or three times daily if needed or as directed by a doctor • if bothersome dryness or peeling occurs, reduce application to once a day or every other day

Regulatory & Marketing

Labeler Name
Tula Life Llc
FDA Application #
part333D
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
12-24-2021
Listing Expiration
12-31-2023
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 72296-040-15 identifies a specific commercial package of 1 tube in 1 carton / 15 g in 1 tube of Tula Skincare Go Away Acne Spot Treatment, labeled by Tula Life Llc. 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 Tula Life Llc on December 24, 2021. The current certification is valid through December 31, 2023.

How is this Tula Life Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72296004015. 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)
72296-040-15
11-Digit CMS (5-4-2)
72296-0040-15

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