Bv Bye Virus 99
Product Images NDC 78501-4000

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Bv Bye Virus 99 (NDC 78501-4000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Comercial Goura,s. De R.l., 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

Label 1000 mL Bye Virus

Label for BV BYE VIRUS 99 hand sanitizer gel by COMERCIAL GOURA, S. DE R.L. The label indicates 33.81 fl oz (1 L) volume and antimicrobial formula with no rinsing required. It includes a drug facts box listing Ethyl Alcohol 70% as the active ingredient and details usage instructions and warnings. The design features blue and white waves and water imagery.*

FDA Label Image

Label 125 mL (Label 125 mL)

Drug Facts panel for BV BYE VIRUS 99 Alcohol Antiseptic 70% Topical Solution. It describes the active ingredient as Ethyl Alcohol 70%, use as antimicrobial hand sanitizer gel non-sterile solution, volume of 125 mL, warnings for external use only and flammability, directions for use, storage information, and inactive ingredients including water, glycerin, carbomer, and triethanolamine. Labeler is Comercial Gouras, S. de R.L., located in Mexico.*

FDA Label Image

Label 19000 mL Bye Virus

Packaging label for BV BYE VIRUS 99 hand sanitizer gel by COMERCIAL GOURA,S. DE R.L. The label emphasizes its antimicrobial formula and no rinsing required. The net weight is 642.466 fl oz (19 L). The label includes Drug Facts with ethyl alcohol as the active ingredient and usage, warnings, directions, and inactive ingredients details. It also features a visual motif of water splashing and icons promoting fast and easy disinfection.*

FDA Label Image

Label 250 mL Bye Virus

BV BYE VIRUS 99 hand sanitizer gel packaging label showing a net weight of 8.5 fl oz (250 ml). The label highlights an antimicrobial formula with no rinsing required and disinfects fast and easy. It includes a Drug Facts panel listing Ethyl Alcohol 70% v/v as the active ingredient and detailed usage, warnings, directions, and ingredient information. The product is manufactured by COMERCIAL GOURA, S. DE R.L. in Mexico, with a visible barcode and flammable liquid warning.*

FDA Label Image

Label 30 mL (Label 30 mL)

Drug Facts panel for BV BYE VIRUS 99 Alcohol Antiseptic 70% Topical Solution, a hand sanitizer gel in a 30 mL container. The label includes the active ingredient, ethyl alcohol 70% v/v, its antimicrobial purpose, directions for use, warnings, storage instructions, and inactive ingredients such as water, glycerin, carbomer, and triethanolamine. The product is made in Mexico by COMERCIAL GOURA,S. DE R.L.*

FDA Label Image

Label 500 mL Bye Virus

Label for BV BYE VIRUS 99 hand sanitizer gel, a 500 ml (16.9 fl oz) bottle by COMERCIAL GOURA, S. DE R.L. The label highlights an antimicrobial formula with no rinsing required and features a Drug Facts panel with active ingredient ethyl alcohol at 70% v/v for antimicrobial use. It includes warnings, directions, and inactive ingredients on a blue background with water wave graphics.*

FDA Label Image

Label 60 mL (Label 60 mL)

Drug Facts panel for BV BYE VIRUS 99 Alcohol Antiseptic 70% Topical Solution. It lists ethyl alcohol 70% as the active ingredient and describes the product as a hand sanitizer gel non-sterile solution, 60 mL. The panel includes uses, warnings, directions, and storage instructions. It also notes inactive ingredients including water, glycerin, carbomer, and triethanolamine, and states the product is made in Mexico by Comercial Goura, S. de R.L.*

* 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.