Active Ingredient(S)
Ethanol 75%
Dalis Hand Sanitizer
FDA Label NDC 77639-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Yongjin Biotechnology Co., Ltd for the product Dalis Hand Sanitizer (NDC 77639-001). 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 - stop use, otc - keep out of reach of children, directions, other information, 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 reduce bacteria that potentially can cause disease
For use when soap and water are not available
Warnings
For external use only -hands
Highly flammable. Keep away from fire or flame
Avoid eyes. In case of eye contact, flush with water
Otc - Stop Use
Discontinue if skin irritation occurs. If condition persists, please consult a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
- Squeeze 1/2 tea spoon amount in you plam then briskly rub hands together thoroughly until dry
Other Information
Store below 104F (40C)
Inactive Ingredients
Water, glycerol, aloe extract
Package Label.Principal Display Panel
Image Description (500ml)
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