Hand Sanitizer
FDA Label NDC 74167-8001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Leidos Biomedical Researh, Inc. for the product Hand Sanitizer (NDC 74167-8001). 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 hand sanitizer labels (front label and drug facts label), otc - purpose, indications & usage, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Purpose

Antiseptic

Warnings

For external use only. Flammable. Keep away from heat or flame

Otc - Do Not Use

  • In children less than 2 months of age
  • On open skin wounds

Otc - Stop Use

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

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.

Dosage & Administration

Directions:

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

Other Safety Information

Other Information:

Store between 15-30c (59-86F)

Avoid freezing and excessive heat above 40 C (104F)

Inactive Ingredient

Inactive ingredients glycerin, hydrogen peroxide, purified water USP

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