Active Ingredient
Ethyl Alcohol 75.0%
Hand Sanitizer
FDA Label NDC 75389-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Huizhou Maxsee Biological Technology Co.,ltd. for the product Hand Sanitizer (NDC 75389-005). 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, purpose, use, warning, precautions, 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
Antimicrobial
Use
Hand Sanitizer to help reduce bacteria on skin
Warning
Flammable, keep away from fire, flame or high temperature
Precautions
For external use only, avoid contact with eves, faces and wounds. If you feel unwell after use, stop using it immediately and consult a doctor
Directions
Pump amount 3 ml- 5 ml into your palms, and spread thoroughly on both hands inside outside, rub onto skin until dry
Other Information
24 months shelf life. Stored in a cool and dry place, avoid direct sunlight or high temperature(below 35 C)
Inactive Ingredients
Water, Aloe Barbadensis leaf juice, Carbomer, Triethanolamine Fragrance, Glycerin,
Otc - Do Not Use
Otc - Stop Use
Otc - Keep Out Of Reach Of Children
Package Label - Principal Display Panel
All Type (All)
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