Kunigel Moisturizing Antiseptic Hand Sanitizer
FDA Label NDC 81941-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Setric Best, S. De R.l. De C.v. for the product Kunigel Moisturizing Antiseptic Hand Sanitizer (NDC 81941-000). 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, use, warnings, do not use, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl alcohol 70%
Purpose
Antiseptic
Use
for hand washing to decrease bacteria on the skin.
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do Not Use
in the eyes
Stop Use And Ask A Doctor If
- irritation and redness develop
- 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
Inactive Ingredients
Water, glycerin, carbomer
Package Labeling: 3.79L
Label (Label)
Package Labeling: 20L
Label2 (Label2)
Package Labeling: 200L
Label3 (Label3)
* Please review the disclaimer below.
