Swagon Hand Sanitizer
FDA Label NDC 72285-106

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Yozzi Co.,ltd for the product Swagon Hand Sanitizer (NDC 72285-106). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Ethyl Alcohol     .................... 70%    v/v

Otc - Purpose

Antiseptic

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

  • Help decrease bacteria on the hands
  • recommended for repeated use.

Warnings

For external use only: hands
Flammable. Keep away from heat or flame.

When using this products

Avoid contact with eyes, in case of contact, rinse with water immediately.

Stop using and ask a doctor if irritation develops.

Other information

  • store under 105℉

Dosage & Administration

Dispense a small amount on palms, rub lightly until dry. Do not rinse.

Inactive Ingredient

Water (aqua), Glycerin, Tocopheryl Acetate, Aloe Barbadensis Leaf Extract

* Please review the disclaimer below.