Altitude Medical Hand Sanitizer
FDA Label NDC 69345-200

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Altitude Medical for the product Altitude Medical Hand Sanitizer (NDC 69345-200). 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, active ingredient, purpose, uses, warnings, when using this product, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

Drug Facts

Active Ingredient

Ethyl alcohol, 69.8% v/v

Purpose

Antimicrobial

Uses

  • Sanitize hands without requiring water or a rinse

Warnings

Flammable

For external use only

When Using This Product

  • Do not use near heat or flame
  • Do not use in or near eyes
  • Discontinue use if irritation and redness develop
  • Do not use on deep or puncture wounds, consult your doctor

Keep Out Of Reach Of Children.

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

  • apply gel liberally to unsoiled hands and rub in thoroughly
  • allow to dry without wiping or rinsing

Other Information

  • Store at room temperature

Inactive Ingredients

Water, glycerin, carbomer, glycereth-7 triacetate, triethanolamine, fragrance and tocopherol acetate.

Package Label.Principal Display Panel

AltitudeMedical

Hand Sanitizer

Kills 99.999% of germs without water!

Net Contents 5/408mL (13.5 Fl oz)

Emergency #

1-888-959-0211

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