Autospritz
FDA Label NDC 79281-010

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Origyn Llc for the product Autospritz (NDC 79281-010). 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 ingredients, inactive ingredients, purpose, keep out of reach of children, indications & usage, warnings, dosage & administration, refill bottle 33.8 fl oz (1l), and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Alcohol 80% v/v

Inactive Ingredients

Glycerin, hydrogen peroxide, purified water USP

Purpose

Antiseptic

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.

Indications & Usage

  • Hand sanitizer to help reduce bacteria that potentially can cause disease.
  • For use when soap and water are not available

Warnings

  • For external use only. Flammable. Keep away from heat or flame.
  • Do not use
    • for children less than 2 months of age
    • on open skin wounds
    • When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
    • Stop use and ask a doctor if irritation of rash occurs. These may be signs of a serious health condition.
    • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using this product to avoid swallowing.

* Please review the disclaimer below.