Otc - Active Ingredient
Ethyl Alcohol 70%
Advanced
FDA Label NDC 52305-940
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 Advanced (NDC 52305-940). 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, otc - keep out of reach of children, dosage & administration, inactive 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
Otc - Purpose
Antimicrobial
Indications & Usage
Hand sanitizer to help reduce bacteria on the skin.
Warnings
Flammable-keep away from fire or flame. For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.
Inactive Ingredient
Water, Isopropyl Alcohol, Isopropyl Alcohol, PEG-12 Dimethicone, Caprylyl Glycol, Glycerin, Propylene Glycol, Isopropyl Myristate, Tocopheryl Acetate, Fragrance.
* Please review the disclaimer below.
