3lab Hydra Day Spf 20 Broad Spectrum Water-based Sunscreen Cream
NDC Package 76159-124-01
Package Information
3lab Hydra Day Spf 20 Broad Spectrum Water-based Sunscreen (octinoxate, octisalate, avobenzone) cream is apply liberally 15 minutes before sun exposureReapplyAfter 40 minutes of swimming or sweatingImmediately after towel dryingAt least every 2 hoursSun 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 a.m. This formulation utilizes a cream delivery system. Marketed by 3lab, Inc, this product is identified by NDC 76159-124 and is authorized under FDA application M020.
Identification & Billing
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 76159 - 3lab, Inc
- 76159-124 - 3lab Hydra Day Spf 20 Broad Spectrum Water-based Sunscreen
- 76159-124-01 - 60 mL in 1 BOTTLE
- 76159-124 - 3lab Hydra Day Spf 20 Broad Spectrum Water-based Sunscreen
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.
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Other Available Packages
The following commercial packages are registered under the same Product NDC (76159-124). 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 76159-124-01 identifies a specific commercial package of 60 ml in 1 bottle of 3lab Hydra Day Spf 20 Broad Spectrum Water-based Sunscreen, a human over the counter drug labeled by 3lab, Inc. This cream is formulated for topical use and contains avobenzone; octinoxate; octisalate 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 3lab, Inc on October 15, 2012. The current certification is valid through December 31, 2026.
How is this 3lab, Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 76159012401. 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 Product segment to maintain the 5-4-2 structure.