Biocence Spray
Product Images NDC 59998-202

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Biocence (NDC 59998-202). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bio-germ Protection Llc, 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

Biocence_1 (Biocence 1)

The BIOCENCE topical spray label by Bio-Germ Protection LLC highlights a multi-use antiseptic spray containing active ingredients Eucalyptol 0.091% and Thymol 0.063%. The label emphasizes its antibacterial and antiviral properties for wound, burn, and ostomy site care. Packaging includes directions, warnings, inactive ingredients, and company contact information.*

FDA Label Image

Biocence_2 (Biocence 2)

This image shows the Drug Facts panel for BIOCENCE spray, a topical antiseptic containing Eucalyptol 0.091% and Thymol 0.063%. It includes uses as an antiseptic for cleaning wounds, warnings for external use only with guidance on use around eyes and wounds, directions for application, storage instructions, and a list of inactive ingredients such as beeswax, castor oil, and various essential oils. Contact information for questions and manufacturer details are also present.*

FDA Label Image

Biocence_3 (Biocence 3)

Drug Facts panel for Biocence Spray with active ingredients Eucalyptol 0.091% and Thymol 0.063%. The label lists uses as a multiple-use antiseptic for frequent use without water to protect against infection. Warnings include external use only, avoiding eyes and large areas, consulting a physician for serious burns or puncture wounds, limiting use to one week unless directed, and keeping out of reach of children. Directions advise cleaning the area, applying product 1 to 3 times daily, bandaging, and drying if bandaged. Additional information includes shaking well before use and storage at 1-50°C. The label also lists inactive ingredients and contact information for questions.*

* 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.