Happ Hand Sanitizer
FDA Label NDC 76735-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Fujian Happiness Biotech Technology Co., Ltd. for the product Happ Hand Sanitizer (NDC 76735-001). 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, inactive ingredients, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 65% v/v.

Purpose

Antiseptic

Uses

  • to decrease bacteria on the skin that could cause disease
  • recommended for repeated use

Warnings

For external use only - hands

  • Flammable, keep away from heat and flame

    • When using the 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 and ask a doctor if skin irritation develops.

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

  • Wet hand thoroughly and allow to dry without wiping
  • For children under 6, use only under adult supervision
  • not recommended for infants

Inactive Ingredients

Purified water, Glycerin, Polyacrylic acid, Aminomethylpropanol

* Please review the disclaimer below.