Active Ingredient
Ethyl alcohol 70% v/v
Perk Hand Sanitizer Moisturizing Gel
FDA Label NDC 80434-280
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Worklifebrands Llc for the product Perk Hand Sanitizer Moisturizing Gel (NDC 80434-280). 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, otc - when using, otc - stop use, otc - 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
To decrease bacteria on the skin
Warnings
Flammable. Keep away from fire or flame.
For external use only
Otc - When Using
When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts
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
- Place enough product in your palm to thoroughly cover your hands
- Rub hands together briskly until dry
- Children under 6 years of age should be supervised when using this product.
Inactive Ingredients
Water (Aqua), Isoproyl Alcohol, Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Glycerin, Isopropyl Myristate, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Fragrance (Parfum), Blue 1 (CI 42090), Yellow 5 (CI 19140)
Package Label.Principal Display Panel
Product Label (24939735 9769 42b3 A516 636935c53b39)
Product Label (24939735 9769 42b3 A516 636935c53b39)
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