One For All Hand Sanitizer
FDA Label NDC 80287-013
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Acatechol, Inc. for the product One For All Hand Sanitizer (NDC 80287-013). 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, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.13%
Purpose
Antiseptic/Antimicrobial
Uses
• For personal hand sanitizing to reduce viruses and bacteria on the skin.
• Recommended for repeated use.
Warnings
For external use only.
Do not use in eyes or mouth. In case of eye contact, flush eyes with water.
Stop use and ask a doctor if skin or eye irritation develop.
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.
Directions
• Dispense 1–2 pumps of foam. • Wet all surfaces of hands thoroughly. • Rub gently for 15 seconds until dry.
Other Information
Store below 110°F (43°C).
Inactive Ingredients
Caffeic Acid, Citric acid, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Octadecyldimethyl (3-Trihydroxysilyl Propyl) Ammonium Chloride, Simmondsia Chinensis (Jojoba) Seed Oil, Urea, USP Water.
Questions
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