Daydream Cushion
Product Images NDC 73586-103

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 Daydream Cushion (NDC 73586-103). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Em Cosmetics Llc, 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

01b Lbl_em_daydream Cushion_spf50_12g_gentle Light_full Size (01b Lbl Em Daydream Cushion Spf50 12g Gentle Light Full Size)

01b Lbl_em_daydream Cushion_spf50_12g_gentle Light_full Size (01b Lbl Em Daydream Cushion Spf50 12g Gentle Light Full Size)
Drug Facts label for DAYDREAM CUSHION GENTLE LIGHT sunscreen from EM Cosmetics LLC. It lists active ingredients Avobenzone 1.5%, Homosalate 8.0%, Octisalate 3.0%, Titanium Dioxide 11.8%, with sun protection purpose. Directions for use, warnings, inactive ingredients, and product information including net weight and refill details are included.*
FDA Label Image

01b Lbl_em_daydream Cushion_spf50_12g_gentle Light_refill (01b Lbl Em Daydream Cushion Spf50 12g Gentle Light Refill)

01b Lbl_em_daydream Cushion_spf50_12g_gentle Light_refill (01b Lbl Em Daydream Cushion Spf50 12g Gentle Light Refill)
Drug Facts panel for DAYDREAM CUSHION GENTLE LIGHT sunscreen by EM Cosmetics LLC includes active ingredients avobenzone 1.5%, homosalate 8.0%, octisalate 3.0%, and titanium dioxide 11.8%. It covers uses for sunburn prevention, warnings for external use only, and detailed directions for application and sun protection measures. The panel also lists inactive ingredients and provides storage and safety information.*

* 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.