Active Ingredient
Ethyl Alcohol 62%
Hand Sanitizer
FDA Label NDC 79734-034
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Callington Inc. for the product Hand Sanitizer (NDC 79734-034). 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, otc - when using, otc - stop use, 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
For hand washing to decrease bacteria on the skin. Recommended for repeated use.
Warnings
Flammable. Keep away from fire or flame. For external use only. Avoid contact with broken skin.
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts.
Keep Out Of Reach Of Children.
If swallowed, get medical help.
Directions
Wet hands thoroughly with product and allow to dry without wiping.
Not recommended for infants.
Children under 6 years of age should be supervised when using this product.
Other Information
- Do not store above 1109F (43℃).
- May discolor some fabrics.
Inactive Ingredients
Water, Aloe Barbadensis Leaf Juice, Maltodextrin, Glycerin, Propylene Glycol, Acrylates/C1O-30 Alkyl Acrylate crosspolymer, Aminomethyl Propanol, Fragrance, Tocopheryl Acetate, Denatonium Benzoate.
Package Label.Principal Display Panel
Image Of Bottle Label (Novogel34oz)
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