Otc - Active Ingredient
Active Ingredients Purpose
Ethyl Alcohol 65%..............................................................Sanitizer
Refresher Liquid
FDA Label NDC 69662-111
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jao Limited for the product Refresher (NDC 69662-111). 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 otc - active ingredient, purpose, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children, dosage and administration, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Uses: To supplement routinehand washing whenever soap and water are unavailable.
Warnings
FOR EXTERNAL USE ONLY
When Using This Product
When using this product keep out of eyes.
Stop Use And Ask A Doctor If
Stop use and ask a doctor if irritation occurs.
Keep Out Of Reach Of Children
Keep out of reach of children.
Dosage And Administration
Press pump over palm. rub briskly until dry.
Other Information
Naturally derived from grapes
Inactive Ingredients
Distilled water, essential oils (Lavender, Tea Tree, Eucalyptus, Geranium, Sage), Glycerine and Glyceryl Polyacrylate, Panthenol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Amino Methyl Propanol, Methyl Glucose Ether Distearate, Aloe Barbadensis, Chamomile & Calendula Extracts
Indications
Use to supplement routine hand washing whenever soap and water are unavailable.
Do Not Use
Discontinue use if irritation occurs.
Ask A Doctor
For External use only
Directions
Press Pump over palm, rub hands briskly.
Image Of Label
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