Cerave Developed With Dermatologists Sunscreen Broad Spectrum Spf 50 Stick
NDC Package 49967-014-01

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

Package Information

Cerave Developed With Dermatologists Sunscreen Broad Spectrum Spf 50 (titanium dioxide, zinc oxide) sticks is •Apply liberally 15 minutes before sun exposure.•Reapply: •After 40 minutes of swimming or sweating•Immediately after towel drying•At least every 2 hours•Children under 6 months: Ask a doctor•Sun Protection Measures. This formulation utilizes a stick delivery system. Marketed by L'oreal Usa Products Inc, this product is identified by NDC 49967-014 and is authorized under FDA application M020.

Identification & Billing

NDC Package Code
49967-014-01
Package Description
13.32 g in 1 BLISTER PACK
Product Code
49967-014
11-Digit Billing Format
49967001401

Clinical Specifications

Proprietary Name
Cerave Developed With Dermatologists Sunscreen Broad Spectrum Spf 50
Non-Proprietary Name
Titanium Dioxide, Zinc Oxide
Substance Name
Titanium Dioxide; Zinc Oxide
Dosage Form
Stick - A dosage form prepared in a relatively long and slender often cylindrical form.
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)
Usage Information
•Apply liberally 15 minutes before sun exposure.•Reapply: •After 40 minutes of swimming or sweating•Immediately after towel drying•At least every 2 hours•Children under 6 months: Ask a doctor•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 other sun protection measures including: •Limit time in the sun, especially from 10 a.m.-2 p.m.•Wear long-sleeved shirts, pants, hats and sunglasses.

Regulatory & Marketing

Labeler Name
L'oreal Usa Products Inc
Product Type
Human Otc Drug
FDA Application #
M020
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-01-2017
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 49967-014-01 identifies a specific commercial package of 13.32 g in 1 blister pack of Cerave Developed With Dermatologists Sunscreen Broad Spectrum Spf 50, a human over the counter drug labeled by L'oreal Usa Products Inc. This stick is formulated for topical use and contains titanium dioxide; 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 L'oreal Usa Products Inc on November 01, 2017. The current certification is valid through December 31, 2026.

How is this L'oreal Usa Products Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49967001401. 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)
49967-014-01
11-Digit CMS (5-4-2)
49967-0014-01

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