Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 50049-105
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 50049-105). 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, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
For hand Sanitizing
Warnings
■For external use only
Flammable. Keep away from fire or flame
When using this product
n Keep out of eyes. In case of contact with eyes
flush thoroughly with water
■Avoid contact with open skin
1 Do not inhale or ingest
Stop use and ask a doctor
If skin iritation or redness develops
Otc - 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
Wet hands thoroughly with product and allow to dry without wiping
Children under 6 years of age use only under adult supervision.
Not recommended for infants
Inactive Ingredients
Water,Glycerin,Butylene Glycol,
Carbomer,Aminomethyl Propanol,Aloe
Barbadensis Leaf Extract.
* Please review the disclaimer below.
