Active Ingredient
Ethyl Alcohol 70%
Ste-medi
FDA Label NDC 77599-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ellamuse Korea for the product Ste-medi (NDC 77599-201). 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, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
Hand Sanitizer to reduce bacteria on the skin
Warnings
For external use only: hands
Flammable, keep away from heat and flame.
When Using This Product
Keep out of eyes. In case of contact with eyes, nise thoroughly with water. Do not inhale or ingest.
Stop Use And Ask A Doctor If
Irritation or redness develops. Condition persists for more than 72 hours.
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. For children under 6, use only under adult supervision. Not recommended for infants.
Other Information
Do not store above 105F. May discolor certain fabrics.
Inactive Ingredients
Water, Sodium Hyaluronate, Chitosan, Allantoin, Hamamelis Virginiana (Witch Hazel) Extract, Carbomer
Package Label
* Please review the disclaimer below.
