Active Ingredients
Ethyl alcohol 62%
Gel Hand Sanitizer
FDA Label NDC 75769-143
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dashpost Ltd for the product Gel Hand Sanitizer (NDC 75769-143). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, warnings, otc - when using, otc - ask doctor, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Warnings
Flammable. Keep away from fire or flame. For external use only.
Otc - When Using
Do not use in eyes. In case of contact with eyes, rinse with water.
Otc - Ask Doctor
Stop and ask a doctor if irritation and redness develop and persist.
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children. If swallowed, get medical help promptly.
Directions
Wet hands thoroughly with product and allow to dry without wiping.
Other Information
Store under 105°F
Inactive Ingredients
Aloe Barbadensis Leaf, Carbomer, Dimethicone, Triisopropanolamine, Water
Package Label.Principal Display Panel
Repackaged & Relabeled by
Dashpost Ltd
Brecksville, Ohio, 44141
www.dashpost.trade
Manufactured in U.S.A.
* Please review the disclaimer below.
