Bcp Hand Sanitizer
Product Images NDC 78252-301

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Bcp Hand Sanitizer (NDC 78252-301). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Best Chance Products, 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

78252-301-07 (1000l)

Drug Facts panel for BCP HAND SANITIZER lists ethanol 65% as the active ingredient and antiseptic as the purpose. It includes uses, precautions, directions, storage instructions, and inactive ingredients such as water, glycerin, propylene glycol, aloe vera, jojoba oil, and green tea extract. The label states the distributor Best Chance Products, LLC, contact details, and manufacturing origin, Korea.*

FDA Label Image

78252-301-05 (1000ml)

Drug Facts label for BCP HAND SANITIZER includes active ingredient Ethanol 65% as an antiseptic. It lists uses for disinfection of hands and skin, and detailed precautions such as avoiding use around eyes and ears and consulting a doctor if irritation occurs. Directions advise applying an appropriate amount and rubbing thoroughly. Storage instructions recommend keeping the container upright at room temperature. Inactive ingredients include Aloe Vera, Jojoba Oil, Glycerin, and Green Tea Extract. The product is distributed by Best Chance Products, LLC.*

FDA Label Image

78252-301-02 (125ml)

Drug Facts panel for BCP HAND SANITIZER by Best Chance Products, LLC. Active ingredient is Ethanol 65%, used as an antiseptic for disinfection of hands and skin. Contains warnings and precautions such as avoiding use on broken skin, contact with eyes, and inhalation of vapor. Includes directions to apply and rub thoroughly. Lists inactive ingredients like aloe vera, jojoba oil, and green tea extract. Storage instructions specify keeping the container upright at room temperature (1-30 °C). Distributed by Best Chance Products, LLC in Costa Mesa, CA.*

FDA Label Image

78252-301-06 (200l)

Drug Facts panel for BCP HAND SANITIZER by Best Chance Products, LLC. Lists ethanol 65% as the active ingredient with antiseptic purpose. It includes uses, precautions, directions, storage instructions, and inactive ingredients such as aloe vera, jojoba oil, glycerin, and green tea extract. Also shows distributor information and a barcode.*

FDA Label Image

78252-301-03 (250ml)

BCP HAND SANITIZER 8.45 oz (250 ml) bottle label by Best Chance Products, LLC, featuring 65% ethanol as the active ingredient. The label highlights antiseptic properties, antiviral benefits of green tea extract, and moisturizing ingredients including aloe vera, jojoba oil, and glycerin. The product is made in Korea and includes drug facts and usage precautions.*

FDA Label Image

78252-301-04 (500ml)

Drug Facts panel of BCP HAND SANITIZER shows active ingredient Ethanol 65% as antiseptic, usage directions, precautions, storage instructions, and a list of inactive ingredients including water, glycerin, propylene glycol, aloe vera gel, jojoba oil, and green tea extract among others. Labeler is Best Chance Products, LLC; product volume is 16.91 oz / 500 mL, made in Korea.*

FDA Label Image

78252-301-01 (60ml)

Drug Facts panel for BCP HAND SANITIZER lists Ethanol 65% as the active ingredient with antiseptic purpose. It includes directions for use, precautions such as avoiding eyes and ingestion, and storage instructions. The panel mentions moisturizing ingredients like Aloe Vera, Jojoba Oil, and Glycerin, along with other inactive ingredients and contact information for Best Chance Products, LLC. The product is made in Korea and the package size is 2.3 oz / 60 mL.*

* 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.