Active Ingredient(S)
75% Ethanol
Sccuss Hand Sanitizer Gel
FDA Label NDC 80035-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Aocai Bio-technology Co., Ltd. for the product Sccuss Hand Sanitizer Gel (NDC 80035-001). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - 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
Highly effective alcohol based hand sanitising gel.
Use anywhere without the need for water.
For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame.
Do Not Use
In children less than 2 months of age.
On open skin wounds.
Otc - When Using
Avoid contact with eyes. In case of eye contact, immediately flush eyes with water.
Do not use on broken or irritated skin.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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 onto hand and rub over palms, back of hands and fingers until dry.
Do not wash after use.
Not recommended for infants.
Other Information
Store in a well-ventilated place. Keep cool.
Inactive Ingredients
Aqua, Glycerin, Fragrance, Triethanolamine, Carbomer, Aloe Vera, Vitamin E.
* Please review the disclaimer below.
