Otc - Active Ingredient
Active Ingredient: Ethyl Alcohol (Denatured)70%
Genius Care Hand Sanitizer
FDA Label NDC 90102-312
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gokul Wholesale, Inc. for the product Genius Care Hand Sanitizer (NDC 90102-312). 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, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose: Antiseptic
Indications & Usage
Use: Hand Sanitizer To Decrease Bacteria On The Skin
Warnings
Caution: If Product Gets Into Eyes, Rinse Well Water Immediately. Discontinue Use If Signs Of Irritation Or Rash Appear. If Swallowed, Seek Medical Assistance.
NO-RINSE FORMULA FOR HAND CARE
- FOR EXTERNAL USE ONLY.
- AVOID CONTACT WITH EYES
Otc - Keep Out Of Reach Of Children
- KEEP OUT OF REACH OF CHILDREN
Dosage & Administration
Usage: Apply Desired Amount To Hands. Rub Together Until Get Dry.
Inactive Ingredient
Contains: Ethyl Alcohol (Denatured)70%, Triethanol Amine, Propylene Glycol, Glycerine, Carbomer Di Sodium Edta & Perfume.
Packaging
Image (90102 31210)
Image (90102 31220)
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