Active Ingredient(S)
1. Alcohol 62% v/v
Play-doh Hand Sanitizer
FDA Label NDC 51522-032
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 Play-doh Hand Sanitizer (NDC 51522-032). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - 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
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 heat or flame
Do Not Use
- in children less than 2 months of age
- on open skin wounds
Otc - When Using
· Do not get into eyes.
· if contact occurs, rinse eyes thoroughly with water
Otc - Stop Use
irritation and redness develop
Otc - Keep Out Of Reach Of Children
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 between 66 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 Acrylates Crosspolymer, Fragrance, Polysorbate 20, Sodium Hydroxide, Red 33
* Please review the disclaimer below.
