Slip Tint Broad Spectrum Spf 35 Sunscreen Tinted Moisturizer Shade Four And Half Cream
Product Images NDC 90086-018

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Slip Tint Broad Spectrum Spf 35 Sunscreen Tinted Moisturizer Shade Four And Half (NDC 90086-018). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clean Beauty For All, Inc (dba Saie), 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

Inner Label6 (Inner Label6)

Inner Label6 (Inner Label6)
Front and back views of a tube of Saie Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Four and Half in cream form, containing 40 mL (1.35 fl oz). The front features the brand name 'saie' prominently, with product details below. The back lists the active ingredient as Zinc Oxide 15%, directions for use, and warnings. The tube is labeled by Clean Beauty For All, Inc, with manufacturing and import details.*
FDA Label Image

Outer Label6 (Outer Label6)

Outer Label6 (Outer Label6)
Packaging label for Saie Slip Tint Broad Spectrum SPF 35 Sunscreen Tinted Moisturizer Shade Four and Half, a cream with zinc oxide (15%) as the active sunscreen ingredient. The label indicates a 40 mL (1.35 oz) tube, distributed by Clean Beauty For All, Inc. The label also includes drug facts, warnings, directions, and a list of inactive ingredients along with certification logos and environmental claims.*

* 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.