Active Ingredient
Ethyl Alcohol 70% v/v.
Holoi
FDA Label NDC 78483-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lifen1 Llc for the product Holoi (NDC 78483-001). 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, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label principle display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Uses
Hand Sanitizer to reduce bacteria on the skin, when water and soap are not available. Recommended for repeated use.
Warnings
For External Use Only.
Flammable. Keep away from fire or flame.
When using this product, avoid contact with eyes. In case of contact, flush eyes with water. Consult a doctor.
Discontinue use if redness or irritation develop. If condition persist form more than 72 hours, consult a doctor.
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.
Directions
Spray as much into your pals and thoroughly spread on both hands. Rub into skin until dry.
Other information
Store at 20 degrees Celsius (66-77 degrees Fahrenheit).
May discolor fabrics.
Inactive Ingredients
Water, Glycerin, Vitamin E, Lemon Grass Essential Oil Blend.
Package Label Principle Display Panel
Image Description (Label12)
* Please review the disclaimer below.
