Otc - Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 65692-2052
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Raining Rose, Inc for the product Hand Sanitizer (NDC 65692-2052). 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 - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, 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
Otc - Purpose
Antiseptic
Indications & Usage
For hand washing to decrease bacteria on the skin.
Warnings
Warnings• For external use only
• Flammable, keep away from fire or flame
• Do not use in eyes. In case of contact, rinse eyes thorougly with water.
• Discontinue use if irritation and redness develop.If condition persists for more than 72 hours consult a doctor.
• Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
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.
Dosage & Administration
Wet hands thoroughly with product and allow to dry without wiping.
Inactive Ingredient
Inactive Ingredients: Aloe Barbadensis Leaf Juice, Denatonium Benzoate, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Water
Package Label.Principal Display Panel
Minicclabel-01 (Minicclabel 01)
* Please review the disclaimer below.
