Total Sanitizer Alcohol Free Foam Hand Sanitizer
FDA Label NDC 80463-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Total Sanitizer, Llc for the product Total Sanitizer Alcohol Free Foam Hand Sanitizer (NDC 80463-001). 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 ingredients, purpose, uses, warnings, do not use, stop use and ask a doctor, 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 Ingredients
Benzalkonium Chloride 0.13%
Purpose
Antimicrobial
Uses
- For hand sanitizing to decrease bacteria on the skin.
- Recommended for repeated use.
Warnings
- For external use only.
Do Not Use
- in eyes. If contact occurs, flush eyes with water.
Stop Use And Ask A Doctor
- if irritation or redness develops. 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.
Directions
- Pump a small amount of foam into palm of hand.
- Wet hands thoroughly with product and allow to dry without wiping.
- Rub hands together briskly until dry.
Inactive Ingredients
Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide.
Package Labeling
Lable (Lable)
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