Daylogic Advanced Hand Sanitizer
FDA Label NDC 11822-4813

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Rite Aid Corporation for the product Daylogic Advanced Hand Sanitizer (NDC 11822-4813). 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, 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

Active Ingredient

Ethyl Alcohol 70% (v/v)

Purpose

Antibacterial

Uses

to help reduce bacteria on the skin.

Warnings

For external use only

  • Flammable
  • Keep away from source of heat or fire

When Using This Product

avoid contact with eyes. If contact occurs, rinse thoroughly with water.

Stop Use And Ask A Doctor If

irritation or redness develops and lasts.

Keep Out Of Reach Of Children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

  • use only to refill a hand sanitizer pump bottle.
  • from the pump bottle, put enough product in your palm to cover hands and rub hands together until dry.
  • children under 6 years should be supervised when using this product.

Other Information

  • store at a temperature below 110°F (43°C).
  • may discolor certain fabrics or surfaces.

Inactive Ingredients

Water (Aqua), Isopropyl Alcohol, Glycerin, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate, Carbomer, Aminomethyl Propanol, Fragrance (Parfum).

Questions Or Comments?

1-866-695-3030

Label Copy

Image Of The Label (21146l)

Image Of The Label (21146l)

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