Cardinal Health Sanitizer
FDA Label NDC 63517-523

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Cardinal Health for the product Cardinal Health Sanitizer (NDC 63517-523). 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 package label.principal display panel, indications & usage, dosage & administration, otc - purpose, otc - keep out of reach of children, warnings, otc - active ingredient, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Package Label.Principal Display Panel

Cardinal Health Aerosol Foam Sanitizer

Indications & Usage

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

Dosage & Administration

Apply approx. 3g

Otc - Purpose

Antimicrobial

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Warnings

Warnings Flammable.Keep away from fire or flame. For external use only When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. Contents under pressure. Do not puncture or incinerate container. Do not store at temperature above 120°F (48°C).

Otc - Active Ingredient

Active ingredient Ethyl alcohol 62.5%

Inactive Ingredient

Inactive Ingredients Water (Aqua), Hydrofluorocarbon 152a, Isobutane, Emulsifying Wax NF, Cetyl Lactate, Steareth-2, Propane, Sodium Benzoate, Sodium Sesquicarbonate, Fragrance (Parfum)

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