Eucerin Advanced Hydration Ultra-light Face Sunscreen Spf 50 Lotion
NDC Package 66800-0375-2
Package Information
Eucerin Advanced Hydration Ultra-light Face Sunscreen Spf 50 (avobenzene 3%, homosalate 10%, octisalate 5%, octocrylene 10%) lotions is ■ apply liberally 15 minutes before sun exposure■ reapply: ■ at least every 2 hours ■ use a water resistant sunscreen if swimming or sweating■ Sun Protection Measures. This formulation utilizes a lotion delivery system. Marketed by Beiersdorf Inc, this product is identified by NDC 66800-0375 and is authorized under FDA application M020.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 66800 - Beiersdorf Inc
- 66800-0375 - Eucerin Advanced Hydration Ultra-light Face Sunscreen Spf 50
- 66800-0375-2 - 50 g in 1 BOTTLE, PLASTIC
- 66800-0375 - Eucerin Advanced Hydration Ultra-light Face Sunscreen Spf 50
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.
Other Available Packages
The following commercial packages are registered under the same Product NDC (66800-0375). Click a package code to view its specific billing and regulatory data.
* 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 66800-0375-2 identifies a specific commercial package of 50 g in 1 bottle, plastic of Eucerin Advanced Hydration Ultra-light Face Sunscreen Spf 50, a human over the counter drug labeled by Beiersdorf Inc. This lotion is formulated for topical use and contains avobenzone; homosalate; octisalate; octocrylene 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 Beiersdorf Inc on November 01, 2024. The current certification is valid through December 31, 2026.
How is this Beiersdorf Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 66800037502. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.