Hand Sanitizer
FDA Label NDC 77890-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Angel Tree Products Inc. for the product Hand Sanitizer (NDC 77890-101). 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(s), purpose, use, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient(S)

ETHYL ALCOHOL 62% W/W

Purpose

Antiseptic

Use

  • For hand sanitizing to decrease bacteria on skin when water and soap are not available.

Warnings

For external use only.

  • Do not use if you are allergic to any of the ingredients.
  • When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water.
  • Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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: (800) 222-1222

Directions

WET HANDS THOROUGHLY WITH THIS PRODUCT AND RUB LIGHTLY UNTIL DRY. DO NOT WIPE OFF OR RINSE.

Other Information

  • Store at room temperature
  • Flammable, keep away from fire or flame.

Inactive Ingredients

WATER, GLYCERIN, LAVENDER OIL

* Please review the disclaimer below.