Brytly Solution/ Drops
Product Images NDC 0065-8596

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Brytly (NDC 0065-8596). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alcon Laboratories, 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

Sample Bottle (Samplelabel)

Label for BRYTLY Apraclonidine Hydrochloride Ophthalmic Solution 0.125%, a redness reliever eye drop. The label notes the bottle size is 0.5 mL (0.02 fl oz). It states the package is not child-resistant and includes storage instructions and tamper-evident information. Manufactured by Alcon Laboratories, Inc.*

FDA Label Image

Bottle Label (5mllabel)

Label for BRYTLY Apraclonidine Ophthalmic Solution 0.125%, redness reliever eye drops. The sterile solution is packaged in a 5 mL (0.17 fl oz) container. Manufactured by Alcon Laboratories, Inc., Fort Worth, TX. Label includes storage instructions (2°C to 25°C) and tamper-evident seal warning.*

FDA Label Image

Carton Label (5mlcarton)

Packaging label for BRYTLY Apraclonidine Ophthalmic Solution 0.125%, redress reliever eye drops in a 5 mL (0.17 fl oz) bottle. The label includes drug facts with active ingredient (Apraclonidine 0.125%) and usage instructions for eye redness relief, as well as warnings and directions. Manufactured by Alcon Laboratories, Inc., the label features a tamper-evident notice, barcode, and contact information for questions.*

FDA Label Image

Sample Carton (Samplecarton)

Packaging label for BRYTLY Apraclonidine Ophthalmic Solution 0.125%, redness reliever eye drops by Alcon Laboratories, Inc. The sample-sized bottle contains 0.5 mL (0.02 fl oz) of sterile solution. Front panel highlights the 12-hour duration and 1-minute onset of action. The label includes drug facts, directions, warnings, inactive ingredients, contact information, and a tamper-evident notice. The NDC is 0065-8596-06, and the product is made in Switzerland.*

* 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.