Active Ingredient
Alcohol Denat. 62%
My Little Pony Hand Sanitizer
FDA Label NDC 51522-040
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gold Orient International Limited for the product My Little Pony Hand Sanitizer (NDC 51522-040). 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, use, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
for hand-washing to decrease bacteria on the skin, only when water is not available
When Using This Product
- do not get into eyes.
- if contact occurs, rinse eyes thorouly with water
Stop Use And Ask A Doctor If
- irritation and redness develop
Keep Out Of Reach Of Children.
if swallowed, get medical help or contact a Poison Control Center right away
Directions
wet hands thoroughly with product and allow to dry without wiping
Other Information
- Store at 68° to 77°F (20°~25°C)
- Do not store above 110°F (43°C)
- You may report a serious adverse reaction to this product to Report Reaction, LLC, PO Box 22, Plainsboro, NJ 08536
Inactive Ingredients
Water, Glycerin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Fragrance, Polysorbate 20, Sodium Hydroxide, Yellow 5, Blue 1.
* Please review the disclaimer below.
