Hand Sanitizer
FDA Label NDC 50049-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Quanzhou Besthope Household Products Co., Ltd. for the product Hand Sanitizer (NDC 50049-001). 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 drug facts, active ingredient, purpose, uses, warnings, 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
Active Ingredient
Ethyl Alcohol 75% v/v
Purpose
Antiseptic
Uses
For Hand Sanitizing
Warnings
■Keep out of eyes. In case of contact with eyes,
flush thoroughly with water
■Avoid contact with open skin
■Do not inhale or ingest
Stop use and ask a doctor
■If skin iritation or redness develops
Keep Out Of Reach Of Children.
■Keep out of reach of children. Children under 6
years of age use only under adult supervision
■Not recommended for infants
Directions
■Wet hands thoroughly with product and allow to dry without wiping
Other Information
1 Do not store above 105°F
1 May discolor some fabrics
Inactive Ingredients
Alcohol, Water (Aqua), Glycerin, Butylene Glycol, Carbomer,
Aminomethyl Propanol, Aloe Barbadensis Leaf Extract
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