Inactive Ingredients
Water (Aqua), Glycertin, Carbomer, Propylene Glycol, Aloe Barbadensis Leaf Extract, Tocopheryl Acetate
Ethyl Alcohol
FDA Label NDC 52305-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Freshorize Ltd for the product Ethyl Alcohol (NDC 52305-001). 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 inactive ingredients, directions, warnings:, warnings, active ingredient, other information, purpose, uses, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Directions
Apply small amount ot hands and rub lightly until dry.
Supervise children in the use of the product.
Warnings:
Flammable. Keep away from fire or flames. For external use only.
Keep out of reach of children.
Avoid contact with eyes.
In case of contact, rinse eyes throroughly with water.
Stop use and ask a doctor if skin irritation develops.
If ingested, get medical help or contact a
Poison Control Centre immediatly.
Warnings
Keep out of reach of children.
Active Ingredient
Ethyl Alcohol 70% v/v
Other Information
Avoid extreme temperatures.
Purpose
Antibacterial
Uses
To decrease bacteria on the skin.
Front Label Area
Requires no water or towels.
Apply small amount to hands and rub lightly until dry.
* Please review the disclaimer below.
