Active Ingredient
Alcohol Denat. 62%
Candyland Hand Sanitizer
FDA Label NDC 51522-019
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 Candyland Hand Sanitizer (NDC 51522-019). 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, warnings, when using this product, stop use and ask a doctor if, 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
Use
Use for hand-washing to decrease bacteria on the skin, only when water is not available.
Warnings
For external use only.
Flammable, keep away from fire and flames.
When Using This Product
- do not get into eyes.
- if contact occurs, rinse eyes thoroughly 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 Posion Control Center right away.
Directions
- wet hands thoroughly with product and allow to dry with wiping
Other Information
- Store at 68 to 77F (20-25C)
- Do not store above 110F (43C)
- 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,
Red 40
* Please review the disclaimer below.
