Foaming Hand Sanitizer Refill Moisturizing Aloe
FDA Label NDC 81527-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bocks Inc for the product Foaming Hand Sanitizer Refill Moisturizing Aloe (NDC 81527-001). 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 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
Benzalkonium Chloride 0.13%
Purpose
Antimicrobial
Uses
• hand sanitizer that helps decrease bacteria on the skin
• recommend for repeated use
Warnings
For external use only, do not use in ears, mouth, or eyes.
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
Children should be supervised when using this product.
Directions
• pour liquid into a foaming dispenser
• pump a small amount of foam into palm of hand
• spread thoroughly on both hands
• rub hands together until dry
Inactive Ingredients
Aloe Juice, Citric Acid, Dimonium Chloride Cocoamidopropyl Hydroxyethyldimonium Chloride, Hydroxypropyl Bis-Hydroxyethyldimonium Chloride,Rose Ether, Sodium Citrate, Water
Package Labeling: 473Ml
Bottle3 (Bottle3)
Package Labeling: 946Ml
Bottle4 (Bottle4)
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