Ifm Hand Sanitizer
FDA Label NDC 80701-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Fssc, Llc for the product Ifm Hand Sanitizer (NDC 80701-000). 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 drug facts, active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v

Purpose

Topical Antimicrobial

Uses

  • to decrease bacteria on skin whenever soap and water is not readily available
  • recommended for repeated use

Warnings

For external use only: hands
Flammable, keep away from fire 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 and redness develop and persists for more than 72 hours

Keep Out Of Reach Of Children.

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

Directions

  • wet hands throughly 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 105F
  • may discolor some fabrics
  • may be harmful to wood finishes and plastics

Inactive Ingredients

Glycerin, PEG-6 (and) AMP-Acrylates / Vinyl-Isodecanoate Crosspolymer, Propylene Glycol, Purified Water

Package Labeling:

* Please review the disclaimer below.