Active Ingredient(S)
Ethyl Alcohol 75% v/v
Hand Sanitizer
FDA Label NDC 80800-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Taizhou Duorui Biotechnology Co., Ltd. for the product Hand Sanitizer (NDC 80800-001). 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, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand sanitizer to help decrease bacteria that potentially can cause disease
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
When using this product, keep out of eyes, ears or mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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 immediate medical help or contact a Poison Control Center right away.
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
Store between 15-30C (59-86F)
Avoid freezing or excessive heat above 40C (104F)
Inactive Ingredients
Glycerin, Triethanolamine, Carbomer 940, Aloe Vera Leaf, Alpha Tocopherol, Water
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