Dosage & Administration
Directions
Place a palmful (5 grams) in one hand. Spread onto both hands to wrist and rub into the skin until dry.
Alcohol Free Hand Sanitizer
FDA Label NDC 51053-500
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sanihealth Products Corporation for the product Alcohol Free Hand Sanitizer (NDC 51053-500). 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 dosage & administration, inactive ingredient, boxed warning, indications & usage, otc - active ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Water (Aqua), Decyl Glucoside, Glycerin, Fragrance, DMDM Hydantoin
Boxed Warning
Warnings:
For external use only.
Keep out of reach of children.
Avoid eye contact. Should contact occur, rinse thoroughly with water.
If swallowed or irritation develops, discontinue use and consult a health care practitioner.
Indications & Usage
Use
Use as part of your daily cleansing routine when soap and water are not available, or to supplement hand washing.
Otc - Active Ingredient
Active Ingredient Purpose
Benzalkonium Chloride 0.12% Antiseptic
Package Label.Principal Display Panel
Label (Handsanitizerlabel)
Mission Linen supply
Mission linen and uniform service
Alcohol free hand sanitizer
benzalkonium chloride 0.12%
High performance alcohol free foam hand sanitizer
1 L (33.8 U.S. OZ)
* Please review the disclaimer below.
