Hand Sanitizer
FDA Label NDC 79185-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Amenity Services, Inc. for the product Hand Sanitizer (NDC 79185-101). 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, keep out of reach of children., directions, inactive ingredients, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol (75%)

Purpose

ANTISEPTIC

Use

  • Hand sanitizer to help reduce bacteria that potentially can cause disease.
  • For use when soap and water are unavailable.

Warnings

Flammable. Keep away from heat and flame.

For external use only. Avoid contact with eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.

Stop use and ask doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • For children under 6, use with adult supervision.
  • Not recommended for infants.

Inactive Ingredients

Purified Water (Aqua), Glycerin, Aloe Barbadensis (Aloe Vera) Leaf Juice, Tocopheryl Acetate (Vitamin E) Oil, Lavandula Angustifolia (Lavender) Oil, Carbomer, Aminomethyl Propanol.

Other Information

  • Store between 15-30C (59-86f). Avoid freezing and excessive heat above 40C (104F).

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