Geneva, March 20 -- International Clinical Trials Registry received information related to the study (CTRI/2026/02/104841) titled 'SPF of Naturis UV Shield Sun Boost (NCL 50149 E)' on Feb. 26.

Study Type: PMS

Study Design: Single Arm Study Method of generating randomization sequence:Not Applicable Method of allocation concealment:Not Applicable Blinding and masking:Open Label

Primary Sponsor: Naturis Cosmetics Pvt. Ltd

Intervention: Intervention1: Test Product: UV Shield Sun Boost (NCL50149 E): Quantity2 mg/sq.cm Route of administration: Topical Frequency: Once Duration: 24 hour Control Intervention1: Reference Sunscreens: Quantity2 mg/sq.cm Route of administration: Topical Frequency: Once Duration: 24 hour

Recruitment Status:...