Otc - Active Ingredient
Active Ingredients - Ethyl Alcohol 70%
Aloe Touch
FDA Label NDC 71020-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sante Manufacturing Inc for the product Aloe Touch (NDC 71020-010). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, instructions for use, other safety information, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose - Antiseptic
Indications & Usage
Use hand sanitizer to help reduce disease causing bacteria on the skin
Warnings
Warnings
Flammable. Keep away from fire or flame
Instructions For Use
For external use only -
Other Safety Information
Avoid contact with eyes. In case of contact, rinse eyes thoroughly with water
Otc - Stop Use
Stop use and ask a doctor if irritation or redeness develops
Otc - Keep Out Of Reach Of Children
Keep out of reach of children
If swallowed, get medical help or contact a POison Control Center right away
Dosage & Administration
Directions
- Apply liberally to hands and rub thoroughly until dry
- supervise children in the use of this product
Inactive Ingredient
Inactive Ingredients
Water, Carbomer, Triethanolamine, Glycerin, Propylene Glycol, Aloe Barbadensis Leaf Juice, Fragrance, FD & C Blue# 1, FD & C Yellow# 5
Package Label.Principal Display Panel
SpaSoap
Hand Sanitizer
Aloe Touch
2oz / 59ml
* Please review the disclaimer below.
