Bq Pharma Hand Sanitizer
Product Images NDC 78817-001

2 FDA label images from Frank Por Laboratories, S.a. De C.v. · 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 Bq Pharma Hand Sanitizer (NDC 78817-001). 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)

Principal Display Panelbqpharmahandsanitizer70 % Ethyl Alcohol3.04 Fl Oz. (Bq Pharma Hand Sanitizer 70 Percent 01)
Drug Facts for BQ Pharma Hand Sanitizer Fresh Scent show 70% Ethyl Alcohol as the active antiseptic ingredient. It includes directions for use, warnings, inactive ingredients, and storage instructions. Additional information advises on proper application, safety precautions, and contact details for questions or comments. The sanitizer contains a mix of moisturizers to keep hands hydrated for up to 24 hours.*
FDA Label Image

Bq Pharma Hand Sanitizer 70 Percent 02

Bq Pharma Hand Sanitizer 70 Percent 02
The image shows the front and back labels of BQ Pharma Hand Sanitizer Fresh Scent by Frank por Laboratories, S.A. de C.V. The front label highlights 70% ethyl alcohol content, claims to kill 99.99% of common germs, features a hydra-nutrition complex, and states it leaves hands feeling soft. The net content is 13.52 fl oz. The back label displays the Drug Facts panel including active ingredient, uses, warnings, directions, other information, inactive ingredients, and a barcode placeholder marked 'FPO'.*

* 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.