Active Ingredient(S)
Ethyl Alcohol 71.5% v/v. Purpose: Antiseptic
Dermokil
FDA Label NDC 75004-786
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Halshe, Llc for the product Dermokil (NDC 75004-786). 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, warnings, do not use, when using this product, stop use, 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, Hand Sanitizer
Warnings
For external use only. Flammable. Keep away from heat or flame
Do Not Use
Do not use on damaged, inflamed or broken skin
When Using This Product
Avoid contact with eyes
In case of eye contact, rinse eyes thoroughly with water
Stop Use
Stop use and ask a doctor if irritation or redness develops and lasts for more than 72 hours.
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
- allow to dry without wiping
Other Information
Other information
- keep out of direct sunlight
- store in dry conditions
Inactive Ingredients
glycerin, isopropyl alcohol, sodium hydroxide, purified water USP
Use
Use for hand sanitizing to decrease bacteria on the skin
Package Label - Principal Display Panel
500 ml NDC: 75004-786-55
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