Otc - Active Ingredient
Active Ingredient:
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 69831-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laser Graphics Inc. for the product Hand Sanitizer (NDC 69831-0001). 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, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose:
Antiseptic
Warnings
Warnings:
Flammable. Keep away from fire or flame.
For external use only. Avoid contact with broken skin.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help.
Dosage & Administration
Directions:
Not recommended for infants. Wet hands thoroughly with product and allow to dry without wiping. Children under 6 years of age should be supervised when using this product.
Inactive Ingredient
Water, Glycerin,Propylene Glycol, Carbomer, Triethanolamine, Aloe barbadenis Leaf Juice, Fragrance
Storage And Handling
Other Information:
Do not store above 110 F. May discolor some fabrics.
Indications & Usage
For hand washing to decrease bacteria on the skin. Recommended for repeated use.
Otc - When Using
When using this product, do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.
Package Label.Principal Display Panel
Image Of Bottle Label (Label Ta)
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