Biolle Tears
Product Images NDC 69994-001

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Biolle Tears (NDC 69994-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sage Ethnographic Research, Dba Bioll�, 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

Image (Biolle 01)

Image (Biolle 01)
An instructional illustration showing two hands holding a small plastic vial with a square indentation, demonstrating where to snap or break it open, likely for dispensing a liquid product such as Biolle Tears.*
FDA Label Image

Image (Biolle 02)

Image (Biolle 02)
An instructional illustration showing a hand holding an eye dropper above an eye, demonstrating the application of eye drops. The image highlights the position for administering Biolle Tears eye drops.*
FDA Label Image

Principal Display Panel (0.6 mL Vial Carton)

Principal Display Panel (0.6 mL Vial Carton)
Packaging label for Biollé Tears preservative-free eye lubricant drops, providing moderate dry eye relief. The label indicates 32 single-use containers, each with 0.02 fl oz (0.6 mL) sterile contents. Manufacturer is SAGE Ethnographic Research, dba Biollé, with a product NDC of 69994-00132. The label includes usage directions, drug facts including active ingredient carboxymethylcellulose sodium 0.5%, inactive ingredients, warnings, and storage instructions. The label also shows the lot and expiration date fields.*

* 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.