Active Ingredient(S)
Ethyl Alcohol 73%.
Hand Sanitizer
FDA Label NDC 78065-2020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Studio 320 for the product Hand Sanitizer (NDC 78065-2020). 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, otc - keep out of reach of children, do not use, otc - stop use, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
For external use only. If swallowed, seek medical help or contact a Poison Control Center immediately.
Use
Reduces bacteria on skin. Use when soap and water are not available.
Warnings
Flammable. Keep away from flame.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Do Not Use
Do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if rash appears.
Directions
Bend where indicated on package to dispense. Squeeze contents into hands and rub together until dry.
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
Water, Glycerin, Hydroxypropyl Cellulose, Tert Butanol, Methanol, Acetaldehyde, 2-Propanol
Package Label - Principal Display Panel
Just Hand Sanitizer Box (Justhandsanitizerfinal1)
Just Hand Sanitizer box
* Please review the disclaimer below.
