Active Ingredients
Active Ingredients
Alcohol 75%
Hand Sanitizer
FDA Label NDC 77204-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shanghai Zuwei Medical Healthcare Instruments Co.,ltd. for the product Hand Sanitizer (NDC 77204-001). 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 ingredients, purpose, use, warnings, do not use, when using this product, stop use and ask a doctor, 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
Purpose
Antiseptic
Use
Use Helps reduce bacteria that potentially can cause disease.
Warnings
Warnings
For external use only. Flammable.
Keep away from heat or flame.
Do Not Use
Do not use
- On children less than 2 months of age
- on open skin wounds
When Using This Product
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
Stop use and ask a doctor if irritation or rash 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
Directions Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Other information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive Ingredients
Inactive ingredients Aloe Vera extract, Carbomer, Glycerol, Triethanolamine, Vitamin E, Water(Purified)
Package Label - Principal Display Panel
100 ml NDC: 77204-001-01
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