Instant Hand Sanitizer Gel
FDA Label NDC 61598-450

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ltc Products Inc. for the product Instant Hand Sanitizer (NDC 61598-450). 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 other, active ingredient, purpose, uses, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

Drug Facts

Active Ingredient

Ethyl Alcohol 62% w/w

Purpose

Antiseptic

Uses

  • hand sanitizer to help reduce bacteria on the skin that could cause disease

Warnings

Flammable. Keep away from fire or flame

For external use only - hands.

Otc - When Using

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a physician if skin irritation or rash develops.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If accidently ingested, seek medical help or contact a Poison Control Center immediately.

Directions

  • place enough product in your palm to thoroughly cover your hands
  • rub hands together briskly until dry
  • children under 6 years of age should be supervised when using this product

Other Information

  • store at normal room temperature
  • may discolor certain fabrics
  • may be harmful to wood finishes and plastics

Inactive Ingredients

carbomer, fragrance, glycerin, isopropyl alcohol, isopropyl myristate, propylene glycol, purified water, tocopheryl acetate, aloe vera gel, AMP-95

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INSTANT

HAND
SANITIZER

KILLS 99.9%

Of Common Harmful Germs


Made in USA

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