Alcohol Free Hand Sanitizer
FDA Label NDC 77042-110
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guide Energy Solutions Llc for the product Alcohol Free Hand Sanitizer (NDC 77042-110). 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 drug facts, active ingredient[s], purpose, use[s], warnings, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient[S]
Benzalkonium Chloride 0.13%
Purpose
Skin Antiseptic
Use[S]
For hand and skin sanitizing to decrease microbes on skin.
Warnings
For external use only. Do not use in the eyes. In case of eye contact, flush thoroughly with water & seek medical attention.
Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.
Directions
Dispense an adequate amount in palm to cover hands.
Rub hands together to cover skin thoroughly until dry.
Supervise young children while using this product.
Other Information
*Skin cells may be shed naturally or by abrasion prior to 4 hours, exposing fresh, unprotected skin. Reapply as needed.
Inactive Ingredients
Water, Calcium Silicate
* Please review the disclaimer below.
