Artemis Alcohol-free Antiseptic Foam Hand Sanitizer
FDA Label NDC 49765-310

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Artemis Bio-solutions, Inc. for the product Artemis Alcohol-free Antiseptic Foam Hand Sanitizer (NDC 49765-310). 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 other, otc - active ingredient, otc - purpose, uses, otc - stop use, 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

Other

Drug Facts

ARTEMIS BIOSOLUTIONS

Manufactured by Artemis BioSolutions.

960 N. Industrial Dr., Ste.4 Elmhurst, IL 60126.

Made in USA.

Otc - Active Ingredient

Active Ingredients

Benzalkonium Chloride 0.13%

Otc - Purpose

Purpose

Antimicrobial

Uses

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

Otc - Stop Use

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

Dosage & Administration

Directions

  • Pump a small amount of foam into palm of hand.
  • Wet hands thoroughly with product and allow to dry without wiping.
  • Rub hands together briskly until dry.

Inactive Ingredient

Inactive Ingredients

Water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance

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