Hand Sanitizer
FDA Label NDC 77352-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Green Planet Industries for the product Hand Sanitizer (NDC 77352-101). 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, purpose, uses, 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

ETHYL ALCOHOL (70% w/v)

Purpose

ANTIMICROBIAL

Uses

HAND SANITIZER TO HELP REDUCE BACTERIA THAT CAN POTENTIALLY CAUSE DISEASE. FOR USE WHEN SOAP AND WATER ARE NOT AVAILABLE.

Warnings

  • FLAMMABLE.
  • KEEP AWAY FROM FIRE OR FLAME.
  • FOR EXTERNAL USE ONLY.

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

    Stop use and ask a doctor if irritation or rash appears and lasts.

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.

Directions

  • Put enough product in your palm to cover hands and rub hands together briskly until dry.
  • Children under 6 years of age should be supervised when using this product.

Other Information

  • Store below 110°F (43°C)
  • May discolor certain fabrics.

Inactive Ingredients

WATER, PEG-8, PROPYLENE GLYCOL, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, TERT-BUTYL ALCOHOL, AMINOMETHYL PROPANOL, TOCOPHERYL ACETATE, DENATONIUM BENZOATE.

* Please review the disclaimer below.