Leader Dry Eye Relief Eye Drops Solution/ Drops
Product Images NDC 70000-0502

2 FDA label images from Cardinal Health 110, Llc. Dba Leader · 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 Leader Dry Eye Relief Eye Drops (NDC 70000-0502). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cardinal Health 110, Llc. Dba Leader, 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 Leader Dry Eye Relief Eye Drops (may 2022 Image Update)

Kc Dl Leader Dry Eye Relief Eye Drops (may 2022 Image Update)
Packaging label for Leader Dry Eye Relief Eye Drops sterile lubricant solution. Contains active ingredients glycerin 0.2%, hypromellose 0.2%, and polyethylene glycol 400 1%. The 0.5 fl oz (15 mL) product is distributed by Cardinal Health 110, LLC, Dublin, Ohio. The label highlights comparison to Visine Dry Eye Relief and includes drug facts, warnings, directions, inactive ingredients, and tamper-evident information.*
FDA Label Image

Kc Dl Leader Dry Eye Relief Eye Drops 15ml Twin Pk (2022 Image Update)

Kc Dl Leader Dry Eye Relief Eye Drops 15ml Twin Pk (2022 Image Update)
Leader Dry Eye Relief Eye Drops packaging label showing an ophthalmic solution with active ingredients glycerin 0.2%, hypromellose 0.2%, and polyethylene glycol 400 1%. The label highlights that the product is sterile and a lubricant, available in 2 bottles of 0.5 fl oz each (total 1 fl oz). Distributed by Cardinal Health, the carton includes Drug Facts, warnings, directions, and a 100% money-back guarantee.*

* 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.