Timesavvy Hybrid Xl Cushion Sun Serum Spf 50 Lotion
Product Images NDC 85241-061

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Timesavvy Hybrid Xl Cushion Sun Serum Spf 50 (NDC 85241-061). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Probetter Usa, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Inner Package (Inner Package)

Inner Package (Inner Package)
The label for Timesavvy Hybrid XL Cushion Sun Serum SPF 50 refill depicts a topical lotion with 0.88 oz (25 g) net weight. Active ingredients shown include Homosalate 10%, Octisalate 3%, Octocrylene 2%, and Zinc Oxide 13.58%. The label provides directions, warnings, and instructions on how to replace the refill. Manufactured for ProBetter USA, Inc., made in South Korea.*
FDA Label Image

Label (Label)

Label (Label)
Packaging label for Timesavvy Hybrid XL Cushion Sun Serum SPF 50, a topical lotion sunscreen. The label states broad spectrum SPF 50 PA+++, net weight 0.88 oz (25 g). Active ingredients include homosalate 10%, octisalate 3%, octocrylene 2%, and zinc oxide 13.58%. Manufacturer is ProBetter USA, Inc., with product made in South Korea.*
FDA Label Image

Outer Package (Outer Package)

Outer Package (Outer Package)
Timesavvy Hybrid XL Cushion Sun Serum SPF 50 is a broad spectrum sunscreen lotion in a 2-pack of 0.88 oz (25 g) each, net weight 1.7 oz (50 g). It features advanced hybrid UV technology with mineral and UV filters. Manufactured for ProBetter USA, Inc., this product includes a puff applicator and is made in South Korea.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.