Burbegel Plus Ud
Product Images NDC 76763-202

3 FDA label images from Bgv, S.r.o. · 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 Burbegel Plus Ud (NDC 76763-202). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bgv, S.r.o., 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

1l Label Back (Burbegel Plus Ud Back)

1l Label Back (Burbegel Plus Ud Back)
Drug Facts panel for Burbegel Plus UD hand sanitizer displays active ingredient as Alcohol 70% v/v with antiseptic purpose. It includes use instructions, warnings about flammability and external use only, directions for application, storage conditions, and lists inactive ingredients glycerin, menthol, and purified water USP. Producer and distributor information is given.*
FDA Label Image

1l Label Front (Burbegel Plus Ud Front)

1l Label Front (Burbegel Plus Ud Front)
The label of Burbegel Plus UD hand sanitizer features the brand name prominently with a blue and white background accented with medical cross symbols. It states the active ingredient as Alcohol Antiseptic 70%, describes the product as a topical, non-sterile solution, and includes flammability warnings. The label indicates a 1-liter container and is produced by BGV, s.r.o.*
FDA Label Image

A5ed6b72 902f B4ee E053 2995a90aa234

A5ed6b72 902f B4ee E053 2995a90aa234
Burbegel Plus UD in a translucent white plastic container with a red screw cap. The front label is primarily blue and white with product name Burbegel Plus in bold letters, hazard symbols, and a barcode. The label includes manufacturer BGV, s.r.o., but no visible strength or dosage form is shown.*

* 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.