Hand Sanitizer
FDA Label NDC 76860-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Taizhou Huangyan Liweir Cosmetic Technology Ltd for the product Hand Sanitizer (NDC 76860-002). 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(s), purpose, use, 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.

Label Section Quick Index

Other

NA

Active Ingredient(S)

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Use

To decrease bacteria on the skin that could cause disease

Recommended for repeated use

Warnings

For external use only.

Flammable

May discolor some fabrics

Harmful to wood finishes and plastics

Otc - When Using

When using this 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

Otc - Stop Use

Stop use and ask a doctor if skin irritation develops

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.

Directions

  • Wet hands thoroughly with product and allow to dry without wiping
  • For children under 6 years of age, use only under adult supervision

Inactive Ingredients

Water, triethanolamin, carbomer, aloe barbadensis (aloe vera) gel, fragrance, propylene glycol, glycerin, tocopheryl acetate (Vitamin E)

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