Active Ingredient
Alcohol 62%
Anti-bacterial Dayoff Hand Sanitizer
FDA Label NDC 82697-221
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ghost Stories for the product Anti-bacterial Dayoff Hand Sanitizer (NDC 82697-221). 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, do not use, when using this product, stop use and ask a doctor, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
Decrease bacteria on hands.
Warnings
Flammable: Keep away from heat of flame.
For external use only.
Do Not Use
- In children less than 2 months of age
- On damaged skin or broken skin
When Using This Product
Avoid contact with eyes. If contact occurs, rinse thoroughly with water.
Stop Use And Ask A Doctor
If irritation and redness develop or increase.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Cente right away.
Directions
- Rub a dime size drop into hands.
Other Information
Avoid freezing and excessive heat above 40 °C (104 °F)
Inactive Ingredients
Water(Aqua), Glycerin, Fragrance (Parfum), Carbomer, Lactose, Cellulose, Propylene Glycol, Hydroxypropyl Methylcellulose, Aminomethyl Propanol, L-Menthol, Jojoba Esters, Tocopheryl Acetate, Ascorbyl Palmitate, Mentha Piperita (Peppermint), Leaf Extract, Pinus Densiflora Leaf Extract, FD&C Yellow No. 5, FD&C Blue No. 1, Ultramarines.
Package Label.Principal Display Panel
Dayoff (Dayoff)
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