Neutrogena Healthy Skin Brightening Eye Perfector Spf 20 - Buff 09
NDC Package 69968-0708-1

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 discontinued by the firm.

Neutrogena Healthy Skin Brightening Eye Perfector Spf 20 - Buff 09 is a . Marketed by Johnson & Johnson Consumer Inc., this product is identified by NDC 69968-0708 and is authorized under FDA application part352.

Identification & Billing

NDC Package Code
69968-0708-1
Package Description
1 APPLICATOR in 1 BLISTER PACK / 4.9 g in 1 APPLICATOR
Product Code
69968-0708
11-Digit Billing Format
69968070801

Clinical Specifications

Proprietary Name
Neutrogena Healthy Skin Brightening Eye Perfector Spf 20 - Buff 09
Dosage Form
-

Regulatory & Marketing

Labeler Name
Johnson & Johnson Consumer 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
06-18-2021
End Marketing Date
04-30-2024
Listing Expiration
04-30-2024
Exclude Flag
D
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 69968-0708-1 identifies a specific commercial package of 1 applicator in 1 blister pack / 4.9 g in 1 applicator of Neutrogena Healthy Skin Brightening Eye Perfector Spf 20 - Buff 09, labeled by Johnson & Johnson Consumer 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 Johnson & Johnson Consumer Inc. on June 18, 2021. The current certification is valid through April 30, 2024.

How is this Johnson & Johnson Consumer Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69968070801. 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 (5-4-1)
69968-0708-1
11-Digit CMS (5-4-2)
69968-0708-01

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