Vista Hypromellose Dry Eye Relief Gel
Product Images NDC 77790-002

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Vista Hypromellose Dry Eye Relief (NDC 77790-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Red Wedding 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

Box For Vista Gel 77790-002-10 (Box Vista Gel Final 09172020)

Label for VISTA Hypromellose Dry Eye Relief Gel, hypromellose USP 0.3% w/v eye drops, lubricating gel in a 10 mL (1/3 fl. oz.) bottle. Label includes Drug Facts with active ingredient, uses, warnings, inactive ingredients, directions for use, storage information, manufacturer details (Red Wedding LLC and Omni Lens Pvt. Ltd.), and a barcode. The product is sterile and intended for ophthalmic use.*

FDA Label Image

Vista Gel Label 241026

Label for VISTA Hypromellose Dry Eye Relief Lubricating Gel, containing 0.3% w/v hypromellose as the active ingredient in a 10 ml (1/3 fl. oz.) ophthalmic gel dosage form. The label includes Drug Facts with active and inactive ingredients, usage directions, warnings, and manufacturer details from Red Wedding LLC and Omni Lens Pvt. Ltd, with the NDC 77790-002-10.*

* 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.