Whole Health Hand Sanitizers
Product Images NDC 69222-000

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Whole Health Hand Sanitizers (NDC 69222-000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Suzhou Jingying Daily Necessities Co., Ltd., 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

Backs (Backs)

Backs (Backs)
Drug Facts panels for whole health Hand Sanitizers 3-pack showing active ingredient Ethyl alcohol 62% with antiseptic purpose. Panels include usage instructions, warnings about flammability and eye contact, directions for application, and a list of inactive ingredients such as deionized water, carbomer, triethanolamine, and fragrance. Each panel is labeled Made in China with an expiration date of 10/2016.*
FDA Label Image

Fronts (Fronts)

Fronts (Fronts)
whole health Instant Hand Sanitizer 0.5 FL OZ (15 mL) bottles in a 3-pack. The image shows three bottles labeled with different scents: Lavender Scent, Aloe, and Regular Scent. Each bottle features the whole health logo and the phrase 'Kills Germs.' The labeler is Suzhou Jingying Daily Necessities Co., Ltd.*
FDA Label Image

Handsanitizer3pk (Handsanitizer3pk)

Handsanitizer3pk (Handsanitizer3pk)
Packaging label for whole health Hand Sanitizers 3-pack by Suzhou Jingying Daily Necessities Co., Ltd. The front panel shows the brand name and scents: Lavender, Aloe, and Regular. The back panel includes Drug Facts, active ingredient (Ethyl alcohol 62%), warnings, directions, and barcode. The package is marked as made in China, with each sanitizer volume 0.5 FL OZ / 15 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.