Dry Eye Nighttime
Product Images NDC 59262-378

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 Dry Eye Nighttime (NDC 59262-378). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Similasan 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

Similasandry Eye Nighttime Gelsterile Gel Eye Drops10 mL / 0.33 Fl Oz (Dry Eye Nighttime Gel 01)

Similasandry Eye Nighttime Gelsterile Gel Eye Drops10 mL / 0.33 Fl Oz (Dry Eye Nighttime Gel 01)
Packaging label for Similasan Dry Eye Nighttime Gel sterile gel eye drops. The label highlights the product's use for dryness, redness, and soothing/moisturizing of dry eyes. It states natural active ingredients, homeopathic origin, and contains 10 ml (0.33 fl oz). Directions and drug facts are detailed, including warnings and inactive ingredients. The label features the Similasan logo, NDC 59262-378-11 barcode, and contact information.*
FDA Label Image

Similasandry Eye Nighttime Gelsterile Gel Eye Drops10 mL / 0.33 Fl Oz (Dry Eye Nighttime Gel 02)

Similasandry Eye Nighttime Gelsterile Gel Eye Drops10 mL / 0.33 Fl Oz (Dry Eye Nighttime Gel 02)
Packaging label for Dry Eye Nighttime by Similasan Corporation. The label is in Spanish and details active ingredients, uses related to eye irritation and dryness, warnings, instructions for use, and storage information. It includes a manufacturer's coupon offering a $1 discount on Similasan products with coupon expiration and barcode. Additional contact information for consumer questions is provided along with inactive ingredients listing.*

* 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.