Active Ingredient
Benzalkonium Chloride 0.12%
Liquid Pro Hand Sanitizer
FDA Label NDC 75774-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Saerom International, Inc. for the product Liquid Pro Hand Sanitizer (NDC 75774-000). 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 active ingredient, purpose, uses, warnings, when using this product, stop use and consult a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
• Hand sanitizer to decrease bacteria on the skin • Recommended for repeated use
Warnings
For external use only
When Using This Product
keep out of eyes. In case of contact, flush eyes with water.
Stop Use And Consult A Doctor If
irritation or redness develops.
Keep Out Of Reach Of Children.
If swallowed, get medical assistance or contact a Poison Control Center immediately.
Directions
• Rub thoroughly over all surfaces of both hands.
• Rub hands together briskly until dry.
Inactive Ingredients
aloe barbadensis leaf extract, fragrance, hydroxyethylcellulose, propylene glycol, water
Package Labeling:75774-000-01
Label (Label)
Package Labeling:75774-000-02
Label2 (Label2)
* Please review the disclaimer below.
