Active Ingredient(S)
Ethyl Alcohol: 75% +/-5% v/v
Hand Sanitizer
FDA Label NDC 56084-026
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Rifeshow Cosmetics Co., Ltd. for the product Hand Sanitizer (NDC 56084-026). 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
Antimicrobial
Use
Hand Sanitizer to help reduce bacteria on skin.
Warnings
- For External Use Only.
- Flammable. Keep Away from fire or flame.
Do Not Use
- on children less than 2 years of age.
- on open wounds/cuts.
Otc - When Using
When Using This Product keep out of eyes, ears and mouth. In case of contact with eyes, rinse thoroughly with water.
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 the Posion Control Center immediately.
Directions
Put enough product in your palm to cover hands and rub hands together briskly until dry. Children under 6 years of age should be supervised when using.
Other Information
- Store below 100℉(43℃)
- May Discolor Certain Fabrics
Inactive Ingredients
Water(Aqua), Glycerin, Carbomer, Aminomethyl Propanol, Aloe Barbadensis Leaf Juice.
Package Label - Principal Display Panel
250ml Back Label (1)
250ml Front Label (2)
250ml Label (250ml)
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