Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 70% v/v
Purpose
Antimicrobial
Imk Hand Sanitizer
FDA Label NDC 73856-545
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Biopontis Inc for the product Imk Hand Sanitizer (NDC 73856-545). 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 otc - active ingredient, otc - keep out of reach of children, otc - stop use, otc - when using, dosage & administration, warnings, inactive ingredient, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Dosage & Administration
DIrections
Put as needed in your palms and rub your hands together briskly until dry
children under 6 years of age should be supervised when using this product
Warnings
Warning
Flammable. Keep away from fire or flame.
For external use only.
Inactive Ingredient
Inactive Ingredients
Water(aqua), Glycerin, Aloe Vera leaf, tromethamine, carbomer
Indications & Usage
Use
Hand sanitized to help reduce bacteria on the skin
Otc - Purpose
Use
Hand sanitized to help reduce bacteria on the skin
Package Label.Principal Display Panel
Package label
* Please review the disclaimer below.
