Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 71089-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Germ Guards Incorporated for the product Hand Sanitizer (NDC 71089-002). 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, warnings, otc - stop use, otc - keep out of reach of children, dosage & administration, inactive ingredient, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antimicrobial
Warnings
Warnings
For external use only.
Flammable. Keep away from fire or flame.
Do not use in or near eyes. If eye contact occurs, flush thoroughly with water and seek medical care.
Avoid contact with broken skin.
Ingestion may cause alcohol poisoning. If ingested, contact a physician or local poison control center.
Otc - Stop Use
Stop use and seek medical attention if irritation or redness occurs.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Dosage & Administration
Directions
- Pour product in hands.
- Rub together
- Let dry
- For children under 6, use only under adult supervision.
Inactive Ingredient
Inactive Ingredients: Water, Aloe Barbadenis Leaf Juice, Glycerin, Propylene Glycol, Carbomer, Triethanolamine, Fragrance
Indications & Usage
Uses
- To decrease bacteria on the skin that could cause disease.
- Recommended for repeated use.
Other Information
Store below 110 F/43 C
Package Label.Principal Display Panel
Image Of Bottle Label (Front)
Image Of Bottle Label (Back)
* Please review the disclaimer below.
