Refresh Lacri-lube Ointment
Product Images NDC 0023-0312

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Refresh Lacri-lube (NDC 0023-0312). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Allergan, 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.

FDA Label Image

Telephone (Refresh Lacri Lube 01)

REFRESH LACRI-LUBE ointment for ophthalmic use, containing mineral oil and petrolatum. The packaging displays the product name prominently along with dosage form and active ingredients. It is labeled as a human OTC drug, manufactured by Allergan, Inc. The label includes usage and storage information and regulatory warnings.*

FDA Label Image

Refresh® Lacri-lube® Lubricant Eye Ointmentointmentfor Nighttimedry Eye Reliefnet Wt. 0.12 Oz (3.5 G) Sterile (Refresh Lacri Lube 02)

Packaging label for Refresh Lacri-Lube ointment, an ophthalmic ointment containing mineral oil 42.5% and white petrolatum 56.8% as active ingredients for eye lubrication. The label features a navy blue background with a water droplet image, stating it soothes irritated, dry eyes overnight. The net weight is 0.12 oz (3.5 g), distributed by Allergan, 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.