Alcohol Free Hand Sanitizer Aerosol, Foam
FDA Label NDC 60933-200
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fuller Industries, Inc for the product Alcohol Free Hand Sanitizer (NDC 60933-200). 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, when using this product, 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 Ingredient
Benzalkonoium Chloride 0.1%
Purpose
Antimicrobial
Uses
- For hand sanitizing to decrease the bacteria on skin.
- Recommended for repeated use
Warnings
For external use only
When Using This Product
avoid contact with eyes In case of eye contact, flush eyes with water.
Stop Use And Ask A Doctor
if irritation or redness develops, or if condition persists for more than 72 hours
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
- Rub thoroughly over all surfaces of both hands
- Rub hands together briskly until dry
Inactive Ingredients:
Water; Lauramine Oxide; Undeceth-7; Disodium EDTA; DMDM Hydantoin; Fragrance; Citric Acid; FD&C Red #33; FD&C Blue #1/
Package Labeling:
Label (Label)
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