Decon Hand Instant Hand Sanitizer Liquid
FDA Label NDC 64307-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Veltek Associates, Inc. for the product Decon Hand Instant Hand Sanitizer (NDC 64307-001). 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 ingredients, purpose, uses, warnings, other, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Ethanol 64.5% (w/w)

Purpose

Antiseptic Handwash

Uses

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

Warnings

Flammable, keep away from fire or flame when using this productFor External Use Only

Other

  • Do not use in eyes.
  • In case of eye contact, flush with water for 15 minutes.
  • Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
  • Avoid contact with broken skin.

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.

Other Information

For Spill/Exposure Emergency Response Service in English, French and Spanish (and 23 other languages), call CARECHEM24 at 866-928-0789.

Inactive Ingredients

Acrylates/C10/30 Alkyl Acrylate Crosspolymer, EDTA, Fragrance, Glycerin, Purified Water and Tetrahydroxypropyl Ethylenediamine.

Questions?

Call 610-644-8335

Package Label.Principal Display Panel

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Image Of Container Label (Decon Hand)

Image Of Container Label (Decon Hand)

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