Equate Eye Drops Dry Eye Relief Solution/ Drops
Product Images NDC 49035-280

2 FDA label images from Wal-mart Stores, Inc. · 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 Equate Eye Drops Dry Eye Relief (NDC 49035-280). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Wal-mart Stores, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Kc Dl Equate Dry Eye Relief 15ml Twin Pk

Kc Dl Equate Dry Eye Relief 15ml Twin Pk
Equate Eye Drops Dry Eye Relief 0.2% Glycerin, 0.2% Hypromellose, and 1% Polyethylene Glycol 400 ophthalmic solution in a 2-pack of 0.5 fl oz (15 mL) bottles, total 1 fl oz (30 mL). The packaging highlights its use as a lubricant to soothe, protect, and moisturize dry eyes. Distributed by Wal-Mart Stores, Inc., the box also includes drug facts, directions, warnings, and storage instructions.*
FDA Label Image

Equate Eye Drops Dry Eye Relief (Kc Dl Equate Eye Drops Dry Eye Relief (revised))

Equate Eye Drops Dry Eye Relief (Kc Dl Equate Eye Drops Dry Eye Relief (revised))
Equate Eye Drops Dry Eye Relief twin pack packaging label featuring a teal and white color scheme. It contains two 0.5 FL OZ (15 mL) bottles totaling 1 FL OZ (30 mL). Active ingredients are Glycerin 0.2%, Hypromellose 0.2%, and Polyethylene Glycol 400 1%, labeled as lubricants. The label compares to Visine Dry Eye Relief and indicates that the product soothes, protects, and moisturizes. The packaging includes drug facts, usage instructions, storage information, contact number, and tamper-evident warnings. Distributed by Walmart Inc.*

* 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.