Soothion Antiseptic Hand Sanitizer
FDA Label NDC 69031-006

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Electrolyzed Innovations, Llc for the product Soothion Antiseptic Hand Sanitizer (NDC 69031-006). 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, otc - 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 0.13%

Purpose

Antiseptic

Uses

  • For hand washing to decrease bacteria on the skin.
  • Recommended for repeated use.

Warnings

For external use only.

When Using This Product

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

Stop Use And Ask A Doctor If

  • irritation and redness develops
  • condition persists for more than 72 hours.

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.

Other Information

  • Store in a cool, dry place below 77°F
  • Protect from heat and light


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