Discover Our Services
Leading the Way in SPF & Sunscreen Testing – Compliant, Reliable, and Trusted by Experts.
SPF Testing - ISO
24444:2019
FDA SPF Testing -
21 CFR 201.327
UVA Protection Testing - ISO
24442:2022
In Vitro UVA Testing - ISO
24443:2021
In Vitro Broad Spectrum Testing -
FDA Method
U.S. Regulatory Requirements
FDA Final Rule (2011) / OTC Monograph M020
In the U.S., sunscreens are regulated as over-the-counter (OTC) drugs. The FDA mandates specific testing protocols for SPF labeling, water resistance claims (40 or 80 minutes), and broad-spectrum protection. Compliance with these regulations is crucial for any SPF testing lab operating in the U.S.
In-Vitro Broad Spectrum Testing
For broad-spectrum claims, the FDA requires in-vitro testing methods, such as critical wavelength analysis, to assess UVA protection.
Why Choose UV Pro Lab?
FDA & ISO Compliant Protocols
Professional, Reliable, and Fast
State-of-the-Art Multiport Solar Simulators
Trained Clinical Staff & GCP-Aligned Practices
Comprehensive Reporting for Regulatory Submission
Conveniently Located in Phoenix, AZ
- Note: UV Pro Lab does not currently offer water resistance testing.
- Note: UV Pro Lab does not currently offer ISO 16217 or ISO 18861 water resistance studies.
- Note: UV Pro Lab does not currently offer ISO 23675:2024 – Double Plate Method (In Vitro)