Steril Wize Antibacterial Foaming Hand Sanitizer
FDA Label NDC 77051-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nostalgia Products Llc for the product Steril Wize Antibacterial Foaming Hand Sanitizer (NDC 77051-004). 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, when using this product, stop use and ask a doctor, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzalkonium Chloride 0.1%

Purpose

Antimicrobial

Use

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

Warnings

For external use only.

When Using This Product

If irritation or redness develops and conditions persist.

Stop Use And Ask A Doctor

If irritation or redness develops and conditions persist.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Pump a small amount of foam into palm of the hand.
  • Rub thoroughly over all surfaces of both hands.
  • Rub hands together briskly unit dry.

Inactive Ingredients

Water, Cetrimonium Chloride, Laurtrimonium Chloride, Dihydroxyethyl Cocamine Oxide, Glycereth-17 Cocoate, itric Acid.

Otc - Questions

In Case of Emergency Call Chemtrec 800-424-9300

Package Labeling:

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