Premium Nature Instant Hand Sanitizer
Product Images NDC 75821-002

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Premium Nature Instant Hand Sanitizer (NDC 75821-002). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Premium Assure Inc, 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

Image Description (70 16oz)

Label of Premium Nature Instant Hand Sanitizer featuring a 70% alcohol content badge, styled with blue and green text stating "Improved Formula." The label includes a logo with a green leaf, "Made in the United States of America" round emblem, and product size as 16 OZ (473 ML). The labeler is Premium Nature, and a Drug Facts panel is visible, detailing ingredients and warnings.*

FDA Label Image

Image Description (8oz)

Label for Premium Nature Instant Hand Sanitizer, 8 oz (236 mL), by Premium Assure Inc. The label highlights the product as an improved formula hand sanitizer containing 70% ethyl alcohol with antimicrobial purpose. It includes usage warnings, directions, inactive ingredients, and features a Made in the USA emblem along with the product barcode and expiration date of June 2023.*

FDA Label Image

New 1g Label

Label for Premium Nature Instant Hand Sanitizer by Premium Assure Inc features 70% alcohol content and a 1-gallon container. The label highlights improved formula, states the product is made in the USA, and includes a Drug Facts panel listing ethyl alcohol 70% v/v as the active ingredient. Additional information includes inactive ingredients, usage warnings, directions, and manufacturer contact details.*

* 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.