United Airlines Liquid
Product Images NDC 52305-601

2 FDA label images from Freshorize Ltd · 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 United Airlines (NDC 52305-601). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Freshorize Ltd, 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

United Airlines Label Alcohol Free Hs Snav Approved 11 11 2020 Fda

United Airlines Label Alcohol Free Hs Snav Approved  11 11 2020 Fda
Label for United Airlines hand sanitizer topical liquid with active ingredient Benzalkonium Chloride 0.13g/100mL. The label has a purple background with white text stating 'Hand sanitizer' and includes the Freshorize Ltd labeler information. Directions, warnings, and ingredient details are listed in small print. The volume is 250mL (8.45 fl oz). The label provides website www.freshorize.com and indicates product use for antibacterial purposes.*
FDA Label Image

B3d7cc9c C2c5 B394 E053 2a95a90a1dd8

B3d7cc9c C2c5 B394 E053 2a95a90a1dd8
United Airlines Hand sanitizer label for a topical liquid product containing Benzalkonium Chloride 0.13 g/100mL. The label features a purple square with white text stating 'Hand sanitizer' and the 'UNITED' logo. It includes dosage form and volume (250 mL, 8.45 fl oz), manufacturer Freshorize Ltd contact details, and directions indicating product use as an antibacterial agent. The label also mentions batch number, manufacture date, use-by date fields, and an illustration for activating an air freshener wick into a fragrance container.*

* 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.