Active Ingredient
Alcohol 62% v/v
Jolo Active
FDA Label NDC 79989-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fusion Accelerate, Llc for the product Jolo Active (NDC 79989-001). 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 ingredient, purpose, use, warnings, directions, other information, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
To sanitize hands without requiring water or a rinse – Kills 99.9% of most common bacteria in 15 seconds
Warnings
For external use only
Flammable
Do not use near heat or flame
Do not use
In children less than 2 months of age
On open skin wounds
When using this product keep out of eyes, ears and mouth, In case of contact with eyes, rinse eyes throughly with water.
Stop use and ask a doctor
if irritation or rash occurs.
They may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away atv 1-800-222-1222
Directions
Apply gel liberally to unsoiled hands and rub in thoroughly
Allow to dry without wiping or rinsing
Other Information
- Store at room temperature.
Inactive Ingredients
Water, Aloe barbadensis Leaf Juice, Carbomer, Diisopropylamine, Glycerin, Isopropyl Myristate, Fragrance, Phenoxyethanol, Tocopheryl Acetate, Yellow 10, Yellow 5, Blue 1.
* Please review the disclaimer below.
