Allergy Eye Relief
Product Images NDC 59262-353

2 FDA label images from Similasan Corporation · 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 Allergy Eye Relief (NDC 59262-353). 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

Principal Display Panelallergy Eyereliefsingle-use Sterile Eye Drops0.4 mL/0.014 Fl Oz Each (Allergy Eye Relief Single Use 01)

Principal Display Panelallergy Eyereliefsingle-use Sterile Eye Drops0.4 mL/0.014 Fl Oz Each (Allergy Eye Relief Single Use 01)
Packaging label for Allergy Eye Relief preservative-free single-use sterile eye drops by Similasan Corporation. The box highlights natural active ingredients and use instructions for relief of itching, burning, watering, and redness. The label includes drug facts, warnings, and directions, emphasizing homeopathic formulation and non-GMO status, with a 20 sterile single-use dropper count.*
FDA Label Image

Principal Display Panelallergy Eyereliefsingle-use Sterile Eye Drops0.4 mL/0.014 Fl Oz Each (Allergy Eye Relief Single Use 02)

Principal Display Panelallergy Eyereliefsingle-use Sterile Eye Drops0.4 mL/0.014 Fl Oz Each (Allergy Eye Relief Single Use 02)
Packaging label for Allergy Eye Relief by Similasan Corporation, presented in Spanish. The label includes active ingredients, product purpose, applications, warnings, instructions for use, additional information, inactive ingredients, and contact information. The label is designed as a folding carton template with multiple panels containing text.*

* 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.