Otc - Active Ingredient
Active ingredient
Ethyl Alcohol 70%
Hand Sanitizer
FDA Label NDC 42509-034
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Wessco International for the product Hand Sanitizer (NDC 42509-034). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, 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
Uses: to help reduce germs on the skin
Warnings
Warnings: For external use only, Flammable, Keep away from fire or flame
Otc - When Using
When using this product: avoid contact with eyes, if contact occurs, rinse thoroughly with water.
Otc - Stop Use
Stop using and ask a doctor: if irritation or redness develops and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children: In case of accidental ingetion, get medical help or contact a poison control center immediately.
Dosage & Administration
Directions: Squeeze a significant amount in your palm and rub hands until fully dry. Rinse free.
Storage And Handling
Other information: Store below 110︒F(43︒C)
Inactive Ingredient
Inactive ingredients
Acrylate/C10-30 Alkyl Acrylate crosspolymer, Aloe Barbadensis Leaf Juice, Aminomethyl propanol，Denatonium benzoate, Fragrance, Glycerin, Maltodextrin, Propylene Glycol, Tocopheryl Acetate, Water.
Package Label.Principal Display Panel
Image Of Bottle Label (34oz)
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