Otc - Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 65692-2068
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 for the product Hand Sanitizer (NDC 65692-2068). 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
Flammable. Keep away from fire and flame. For external use only. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor. 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
Dosage & Administration
Wet hands thoroughly with product and allow to dry without wiping.
Inactive Ingredient
Water, Propylene Glycol, Glycerin, Fragrance, Aloe Barbadensis Leaf Juice, Essential Oil.
Package Label.Principal Display Panel
C10876 (C10876)
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