Hand Sanitizer
FDA Label NDC 74341-191

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Newacme Llc for the product Hand Sanitizer (NDC 74341-191). 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, when using this product, stop use or ask a doctor, 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

Active Ingredients

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses:

For Hand Sanitizing

Warnings:

For external use only-hands.

Other

Flammable.  Keep away from heat and 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 Or Ask A Doctor

if skin irritation develops.

Keep Out Of Reach Of Children.

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

Directions:

  • Wet hands thoroughly with a 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 105 oF.  May discolor some fabrics.  Harmful to wood finishes and plastics.

Inactive Ingredients:

Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl ACetate, Triethanolamine, Water.

Package Labeling: 74341-191-08

236ml (74341 191 08)

236ml (74341 191 08)

Package Labeling: 74341-191-16

473ml (74341 191 16)

473ml (74341 191 16)

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