Active Ingredient(S)
Alcohol 70% . Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 61354-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Oxygen Development, Llc for the product Hand Sanitizer (NDC 61354-015). 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(s), purpose, use, warnings, when using this product, 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
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria on the skin.
To decrease bacteria on the skin when water &soap is not available. Recomended for repeated use
Warnings
Flammable. Keep away from heat or flame.For external use only.
When Using This Product
When using this product do not use in or near the eyes. In case of contact, rinse eyes throughly with water.
Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep Out Of Reach Of Children.
Keep out of reach of children. If swallowed, get medical help or contact a or contact a Poison Control Center right away.
Directions
- Place enough product in your palm to cover hands and rub hands together until dry.
- Children under 6 years of age should be supervised when using this product.
Other Information
- Store below 110F(43C).
- May discolor certain fabric surfaces.
Inactive Ingredients
Water/Aqua, Glycerin, Carbomer, Aminomenthyl Propanol, Aloe Barbadensis Leaf Juice.
Package Label - Principal Display Panel
1 (Art 050 Lbl Wrp 079)
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