Active Ingredient
Alcohol 70%
Hand Sanitizer
FDA Label NDC 61354-024
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 61354-024). 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 this product, stop use and ask doctor, 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
Use
For handwashing to decrease bacteria on the skin.
Warnings
Do not eat or drink. Topical application only. Flammable. Keep away from fire 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 troroughly with water.
Stop Use And Ask Doctor
Stop use and ask doctor if irritation or rash persists.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a poison Control Center right away
Directions
Put enough product in your palm to cover hands & rub hands together until dry. Children under 6 years of age should be supervised when using this product
Other Information
store below 110 F (43 C). May discolor certain fabric surfaces.
Inactive Ingredients
Water/Aqua, Glycerin, Fragrance, Polysorbate 20, Carbomer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice
* Please review the disclaimer below.
