Sannytize Hand Sanitizer
FDA Label NDC 67777-317

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dynarex Corporation for the product Sannytize Hand Sanitizer (NDC 67777-317). 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, warnings, purpose, indications & usage, dosage & administration, keep out of reach of children, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Active Ingredient                         Purpose

Ethyl Alcohol 0.62%                   Antiseptic Handwash

Warnings

  • For external use only
  • Flammable, keep away from fire and flame
  • Do not use in or near the eyes
  • When using this product avoid contact with eyes. In case of eye contact, rinse with water to remove.
  • Stop use and ask a doctor if irritation andredness develops

Purpose

An antiseptic handwash.

Indications & Usage

Cleaning and antiseptic cleansing of hands and skin.

Dosage & Administration

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

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.

Inactive Ingredients

Inactive ingredients: Water, Glycerin, Propylene glycol, Carbomer, Triethanolamine, Aloe barbadensis juice, Fragrance

Principal Display Panel

Dynarex SannyTize Hand Sanitizer

hand sanitizer.jpg

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