Helios Hand Sanitizer
Product Images NDC 74140-200

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Helios Hand Sanitizer (NDC 74140-200). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pretty Woman 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

Label Hhs19 80ml Base (Label Hhs19 80ml Base)

A text panel providing directions for use, other information, and a list of inactive ingredients for HELIOS Hand Sanitizer. Directions include wetting hands thoroughly and drying, use only under adult supervision for children under 6, and not recommended for infants. Other information covers storage below 104°F (40°C) and a warning about possible discoloration of fabrics or surfaces. Inactive ingredients listed are acrylates copolymer, aminomethyl propanol, fragrance, glycerin, and water.*

FDA Label Image

Label Hhs19 80ml Inside (Label Hhs19 80ml Inside)

Drug Facts panel for HELIOS Hand Sanitizer provides warnings and precautions including avoiding eye contact, not using on broken skin, and not inhaling or ingesting. It advises stopping use and consulting a doctor if irritation or redness develops or persists beyond 72 hours. It also instructs to keep out of reach of children and seek medical help if swallowed.*

FDA Label Image

Label Hhs19 80ml Pdp (Label Hhs19 80ml Pdp)

HELIOS Hand Sanitizer packaging label by Pretty Woman LLC, containing 2.7 fl. oz. (80 mL) topical solution with 75% ethyl alcohol as the active ingredient. The label includes a Drug Facts panel detailing antiseptic use and warnings for external use only, flammability, and fire safety precautions.*

* 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.