Daylogic Foaming Sanitizer Aloe
FDA Label NDC 11822-2440

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 Foaming Sanitizer Aloe (NDC 11822-2440). 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

Benzalkonium Chloride 0.1%

Purpose

Antiseptic

Uses

to help decrease bacteria on the skin.

Warnings

For external use only

When Using This Product

avoid contact with eyes. If contact occurs, rinse eyes 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

  • Pump enough product on your palm to thoroughly cover your hands, rub together until dry.
  • Children under 6 years should be supervised when using this product.

Inactive Ingredients

Water (Aqua), Polysorbate 20, Ethylhexyl Methoxycinnamate, Buty Methoxydibenzoylmethane, Ethylhexyl Salicyalte, PPG-26-Buteth-26, PEG-40 Hydrogenated Castor Oil, Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Camellia Sinensis Leaf Extract, DMDM Hydantoin, Sodium Hydroxide, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (CI 42090), Yellow 5 (CI 19140).

Label Copy

Image Of Label (21020l)

Image Of Label (21020l)

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