Sentinel Hand Sanitizer
FDA Label NDC 79041-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Danlab Danuta Katrynska for the product Sentinel Hand Sanitizer (NDC 79041-001). 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, otc - keep out of reach of children, directions, other information, inactive ingredients, 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% v/v.

Purpose

Antiseptic

Use

  • To decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use.

Warnings

For external use only:hands.

Flammable. Keep away from heat or flame.

When using this product

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not inhale or ingest.
  • Stop use and ask a doctor if
  • irritation or redness develops.
  • Condition persists for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6, use only under adult supervision.
  • Not recommended for infants.

Other Information

  • Do not store above 1050F
  • May discolor certain fabrics.
  • Harmful to wood finishes and plastics

Inactive Ingredients

Water (Aqua), Isopropyl alcohol, Thickener, Plant pharma glycerin, Peppermint oil.

Package Label - Principal Display Panel

Label 1 (Label1)

Label 1 (Label1)

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