Bq Pharma Hand Sanitizer
Product Images NDC 78817-002

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Bq Pharma Hand Sanitizer (NDC 78817-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Frank Por Laboratories, S.a. De C.v., 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

Principal Display Panelbqpharmahandsanitizer70 % Ethyl Alcohol3.04 Fl Oz. (Bq Pharma Hand Sanitizer 70 Percent 01)

This is a description of a hand sanitizer manufactured in Mexico. It contains 70% ethyl alcohol and can kill 99.99% of common germs. The drug facts section lists the active ingredient as ACOROI70% V... Anlisepic and states that it is intended to reduce bacteria that can cause disease. The sanitizer is flammable and should not be used near heat or flame. Other instructions include avoiding contact with eyes and seeking medical help if a rash occurs. The inactive ingredients include camphor, carbrre, Gicen, Nefihal, Treranoamig, and Water. The product is distributed by O0O0000XK and its purpose is to keep hands moisturized for up to 24 hours.*

FDA Label Image

Bq Pharma Hand Sanitizer 70 Percent 02

This appears to be a label of a drug containing Ethyl alcohol with 70% concentration. It seems to have a warning about inflammability and is not to be used near flames or open wounds. It warns against ingestion and suggests calling a doctor if accidentally ingested. The directions for use are also provided. The label includes information about storage and inactive ingredients used in the product. No further information to evaluate.*

* 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.