SPF Testing

SPF test, UVA test
Cosmetics Testing Laboratory

SPF Testing for Sunscreens: Tests Scope, Methodology & Standards Compliance

Sunscreen products are designed to offer reliable protection against both UVA and UVB radiation, helping to prevent sunburn, premature skin aging, and long-term skin damage. The effectiveness against UVB rays, which are the primary cause of sunburn, is measured by the Sun Protection Factor (SPF).

In contrast, protection against UVA rays—which penetrate deeper into the skin and contribute to photoaging and cellular damage—is assessed using the UVA Protection Factor (UVA-PF). Accurate testing of both SPF and UVA-PF is essential to verify product performance, meet global regulatory standards, and ensure correct product labeling for consumer safety and trust.

These validated testing methods play a critical role in the development, marketing, and regulatory approval of sun care formulations.

SPF Testing, In vivo SPF Test, In vitro UVA test, In vivo UVA test, Water Resistance test, Sunscreen Testing Laboratory

SPF Testing Services Performed in Our Laboratory:

  1. In vivo SPF Test – This test determines the Sun Protection Factor (SPF) of a product by assessing its effectiveness in preventing UVB-induced erythema on human skin. It is conducted under controlled conditions according to international standards such as ISO 24444.
  2. In vivo UVA Test – PPD (Persistent Pigment Darkening) – The PPD method measures the UVA protection level of a sunscreen based on the skin’s pigment darkening response after UVA exposure. It is widely used in regulatory frameworks such as the European Commission’s guidelines, ISO 24442
  3. In vitro UVA-PF Test – This test evaluates the UVA Protection Factor (UVA-PF) by measuring the absorbance of UV radiation through a sunscreen-applied substrate. It is performed in compliance with ISO 24443 and does not require human testing.
  4. Broad Spectrum Protection (In Vitro) – The test verifies that a product offers balanced protection against both UVA and UVB radiation. It is typically conducted using in vitro spectral absorbance analysis, meeting FDA or ISO broad-spectrum criteria.
  5. Water Resistance Test (ISO or on the basis of FDA Guidelines) – This test assesses the product’s ability to maintain its SPF after water immersion, simulating real-life water exposure. It is carried out in accordance with either ISO 16217/18861 or FDA water resistance protocols (40 or 80 minutes).
  6. Sweat Resistance / High Sweat Resistance (In Vivo) – The test measures a product’s efficacy in maintaining UV protection during and after exposure to sweating conditions. It is performed on human volunteers under controlled environmental conditions to simulate high perspiration.
  7. ANTI-SAND Test (Sand Resistance for SPF) – This test evaluates the product’s ability to resist sand adhesion and maintain its SPF after contact with sand. It simulates real-world beach conditions to assess product performance in sandy environments.
  8. Phototoxicity Test (In Vivo) – This test determines whether a product induces toxic skin reactions when exposed to sunlight. It involves applying the product to human skin followed by controlled UV exposure.
  9. Photoallergenicity Test (In Vivo) – The test assesses the potential of a product to trigger allergic skin reactions upon exposure to UV radiation. It is performed on human subjects using a photo-patch testing protocol.

Turnaround Times:

  • in vivo SPF test – results up to 10 days
  • in vitro UVA test – results in 10 days

Our SPF Testing Laboratory performs tests in accordance with:

Contact Us

If you have any questions about the testing methods listed above or would like to request a quote, please don’t hesitate to contact our team.
We’re here to provide guidance and support tailored to your formulation, regulatory market, or development stage.

E-mail: SPF@epidermlab.pl

EpiDermLab Laboratorium badawcze s.c., Poland, 30-613 Kraków, Łowienicka 14/3, VAT-ID: PL9452271009, phone: +48 662 178 533, e-mail: SPF@epidermlab.pl