Active Ingredient(S)
Ethyl Alcohol 75% Purpose: Antiseptic
Cleanslate
FDA Label NDC 75601-1003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Punch Studio, Llc for the product Cleanslate (NDC 75601-1003). 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, do not use, when using this product, stop use and ask a doctor if, 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
Use
To help reduce bacteria on hands when water & soap are not available
Warnings
For external use only
Flammable, keep away from heat or flame
Do Not Use
Do not use
- On children less than 2 years old
- On open skin wounds
When Using This Product
When using this product keep out of eyes, ears & mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
Stop use and ask a doctor if skin irritation occurs.
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 onto hands thoroughly, rub together until dry
- Supervise children under 6 years old
Other Information
- Store between 15-30°C (59-86°F)
- Avoid freezing and excessive heat above 40°C (104°F)
Inactive Ingredients
Water, Aminomethyl Propanol, Carbomer, Glycerin, Propylene Glycol, Aloe Barbadensis Extract, Tocopheryl Acetate
Package Label - Principal Display Panel
30 mL NDC: 75601-1270-1
Front & Back Labels (Fragrance Free Front Back Labels)
Outer Box (Fragrance Free Box)
* Please review the disclaimer below.
