Buildable Blur Cream
Product Images NDC 68577-127

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Buildable Blur (NDC 68577-127). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

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

FDA Label Image

Tube_artwork (200373 Buildablecccream Tube Co21024 1)

Packaging label for Buildable Blur CC Cream by COSMAX USA, CORPORATION. The tube label is turquoise with yellow and white text prominently displaying the product name, Buildable Blur, and identifying it as a broad spectrum SPF 40 sunscreen cream. The label includes active ingredients—Homosalate 9%, Octisalate 4.5%, and Zinc Oxide 7.8%—dosage form as cream, net volume of 1 fl oz/30 mL, and application instructions. Additional instructions, warnings, and company information appear on the back panel. The label design includes clear printing areas and specific color specifications for turquoise Pantone 3272 C, white, and yellow on an aluminum silver foil tube.*

FDA Label Image

Outer Pkg (T100899 Buildableblurcccream 160light Uc11024 1)

Packaging label for Buildable Blur CC Cream 160 Light by Thrive Causemetics, a topical cream with broad spectrum SPF 40 sunscreen. The label highlights active ingredients including Homosalate, Octisalate, and Zinc Oxide, and notes the Blur Effect Technology for color-correcting coverage. The 1 fl oz (30 mL) carton includes usage directions, warnings, inactive ingredients, and product claims such as dermatologist-tested and paraben- and sulfate-free. The labeler is COSMAX USA, CORPORATION.*

* 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.