Dry Eye Nighttime
Product Images NDC 53799-378

2 FDA label images from Similasan Ag · 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 53799-378). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Similasan Ag, 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, 10 ml (0.33 fl oz). The label highlights use for dryness and redness relief with natural active ingredients in a homeopathic original Swiss formula. Directions, warnings, inactive ingredient list, and contact information are included, along with bilingual English and Spanish text. The label notes use as often as needed and features the Similasan logo.*
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 Similasan Dry Eye Nighttime eye drops, displaying active ingredients including Belladonna and Euphrasia officinalis, with application instructions and warnings in Spanish. The label describes a 15X Mercurius solubilis ingredient and provides usage directions, storage information, inactive ingredients, and contact details for Similasan AG. The package also includes a manufacturer coupon offering a $1 discount on Similasan products.*

* 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.