Gc Jeremiah Brent Hand Sanitizer
Product Images NDC 72496-1122

View Photos of 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 Gc Jeremiah Brent Hand Sanitizer (NDC 72496-1122). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Naturich Labs, 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 Panel Part 1 (Gc Jeremiah Brent Hand Sanitizer Gel 1.9oz (back 1of2))

Principal Display Panel Part 1 (Gc Jeremiah Brent Hand Sanitizer Gel 1.9oz (back 1of2))
Drug Facts panel of GC Jeremiah Brent Hand Sanitizer by Naturich Labs. The panel lists the active ingredient as ethyl alcohol 62%, mentions its use to help decrease bacteria, and includes warnings for external use only. A barcode, manufacturing details, and 'Made in the USA' text are also visible at the bottom of the label.*
FDA Label Image

Principal Display Panel Part 2 (Gc Jeremiah Brent Hand Sanitizer Gel 1.9oz (back 2of2))

Principal Display Panel Part 2 (Gc Jeremiah Brent Hand Sanitizer Gel 1.9oz (back 2of2))
Drug Facts label continues with warnings to keep the flammable product away from fire or flame, avoid contact with eyes and broken skin, and stop use if irritation occurs. It advises keeping the product out of children's reach and seeking medical help if swallowed. Directions include squeezing a small drop and caution for use in children under 6 years, not recommended for infants. Inactive ingredients section lists aloe barbadensis, caprylyl glycol, bergamot oil, coconut oil, natural fragrances, lavender, and others.*

* 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.