Antiseptic Hand Sanitizer
FDA Label NDC 73802-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Commonwealth Homes, Inc. for the product Antiseptic Hand Sanitizer (NDC 73802-101). 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 drug facts, active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient

Ethyl alcohol 70%

Purpose

Antiseptic

Uses

  • hand sanitizer to decrease bacteria on skin
  • recommended for repeated use
  • for use when soap and water are not available

Warnings

Flammable, keep away from fire/flame

For external use only

Do not use

  • on children less than 2 months of age
  • on open wounds
  • When using this product do not get into eyes. In case of contact, rinse eyes thoroughly with water

    Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists 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 Centre right away

Directions

  • wet hands thoroughly with product and allow to dry without wiping
  • supervise children under 6 years of age when using this product to avoid swallowing

Other Information

  • store under 105°F

Inactive Ingredients

Hydroxyethyl cellulose, Isopropyl myristate, Propylene glycol, Water

Questions?

1-937-848-2098

You can also report serious side effects to this phone number. Mon - Fri 9.00am - 5.00 pm

Packaging

Image Description (Label2.1)

Image Description (Label2.1)

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