Archstone Hand Sanitizer
FDA Label NDC 75531-016

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Ounuo Cosmetics Co., Ltd. for the product Archstone Hand Sanitizer (NDC 75531-016). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Alcohol     .................... 75%         

Otc - Purpose

Antiseptic

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away.

Indications & Usage

  • 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 or flame.

When using this products

  • 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 using and ask a doctor if irritation develops.

    Other information

    • do not store above 105℉
    • may discolor some fabrics
    • harmful to wood finishes and plastics

Dosage & Administration

  • Wet hands thoroughly with product and allow to dry without wiping.
  • for children under 6, use only under adult supervision
  • not recommended for infants

Inactive Ingredient

Water (aqua), propylene glycol, Glycerin, acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl Propanol, fragrance (parfum).

* Please review the disclaimer below.