Active Ingredient
Ethyl Alcohol 70% v/v
Hand Sanitizer
FDA Label NDC 79995-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Strategic Orient Sourcing Limited for the product Hand Sanitizer (NDC 79995-002). 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, do not use, when using this product, stop use and see a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
- Helps reduce bacteria that potentially can cause disease.
- Helps prevent cross contamination by hand contact.
- Recommended for repeated use.
Warnings
For external use only.
Flammable. Keep away from heat or flame.
Do Not Use
- On children less than 2 months of age or on open skin wounds.
When Using This Product
- Keep out of eyes and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop Use And See A Doctor
if irritation or redness develops.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact a Poison Control Center right away.
Directions
- Place enough product on hands to cover all surfaces.
- Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Avoid freezing and excessive heat above 40°C(104°F).
- May discolor certain fabrics.
Inactive Ingredients
Water, Glycerin, Aloe Barbadensis Extract, Aminomethyl Propanol, Carbomer, Fragrance, Tocopherol.
Package Labeling:500Ml
Label (Label)
Package Labeling:1000Ml
Label2 (Label2)
* Please review the disclaimer below.
