Klinare Hand Sanitizer
Product Images NDC 78342-003

2 FDA label images from Qu�mica Blantex, 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 Klinare Hand Sanitizer (NDC 78342-003). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Qu�mica Blantex, 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

Back 500ml (78342 003 01 Klinare 500 mL Back)

Back 500ml (78342 003 01 Klinare 500 mL Back)
Drug Facts panel for Klinare Hand Sanitizer displaying active ingredient Ethyl alcohol 70% v/v as an antiseptic. It includes warnings about flammability, usage restrictions for children under 2 months and on open wounds, and instructions to avoid contact with eyes. Directions for use advise applying enough product to cover hands and supervising children under 6 years. Storage instructions specify temperatures between 15-30°C and caution against freezing or excessive heat. Inactive ingredients listed include purified water, carbomer, alkyl lactate, propylene glycol, fragrance, aminomethyl propanol, chamomilla recutita extract, tocopheryl acetate, and limonene. Contact phone number and distributor address in New Hyde Park, NY, are also shown.*
FDA Label Image

Pdp 500ml (78342 003 01 Klinare 500 mL Front)

Pdp 500ml (78342 003 01 Klinare 500 mL Front)
Label for Klinare Hand Sanitizer containing 70% alcohol, with citrus scent, vitamin E, and chamomile. The net volume is 16.9 fl oz (500 mL). The label features teal and white design elements, a stylized virus icon, and a QR code for more information. The labeler is Química Blantex, S.A. de C.V.*

* 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.