Otc - Active Ingredient
Ethyl Alcohol 70% v/v
Dermamed Natural Hand Sanitizer
FDA Label NDC 69711-800
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Biological Health Group for the product Dermamed Natural Hand Sanitizer (NDC 69711-800). 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, otc - when using, warnings, indications & usage, 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
Otc - When Using
Hand sanitizer to help reduce bacteria on the skin that could cause disease
Recommended for repeated use
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
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Indications & Usage
Place enough product in your palm to thoroughly cover your hands
Rub hands together briskly until dry
No rinsing required
No towels needed
Inactive Ingredient
Water, Aloe Vera Juice, Glycerin, Isopropyl Myristate,Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Aminomethyl Propanol, Propylene Glycol, Fragrance
* Please review the disclaimer below.
