Active Ingredient
ACTIVE INGREDIENT
Ethyl alcohol …….. 70% v/v
Altitude Medical Hand Sanitizer
FDA Label NDC 69345-300
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Altitude Medical for the product Altitude Medical Hand Sanitizer (NDC 69345-300). 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, when using, stop use, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
PURPOSE
Antiseptic
Use
Hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable. Keep away from heat or flame.
For external use only: hands
When Using
When using this product do not use in or near eyes.
In case of contact, rinse eyes thoroughly with water.
Stop Use
Stop use and ask a doctor if irritation or rash occurs and lasts.
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
• Place enough product in your palm to cover hands and rub hands together briskly until dry.
• Children under 6 years of age should be supervised when using this product.
Other Information
• Store below 100°F (43°C)
• May discolor certain fabrics or surfaces.
Inactive Ingredients
Glycerin, isopropyl alcohol, PEG-6 (and) AMP-acrylates/vinyl isodecanoate crosspolymer, purified water
* Please review the disclaimer below.
