Active Ingredient
Ethyl Alcohol 70% v/v.
Hand Sanitizer
FDA Label NDC 77106-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Resource Recovery & Trading Llc for the product Hand Sanitizer (NDC 77106-001). 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, otc - keep out of reach of children, directions, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
to help reduce bacteria on the skin.
Warnings
Flammable. Keep away from heat or flame. For external use only.
When using this product avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.
Stop using and ask doctor if irritation or rash appers and lasts.
Otc - 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
Apply a small amount in your palm and rub hands together briskly until dry.
Children under 6 should be supervised when using this product.
Other information
Do not store above 110°F (43°C).
Inactive Ingredients
Purified water, carbomer, triethanolamine, glycerin, propylene glycol, fragrance, Aloe Barbadensis leaf juice.
Product Label
* Please review the disclaimer below.
