Amoveo Original
FDA Label NDC 49955-701

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Protair-x Health Solutions Inc. for the product Amoveo Original (NDC 49955-701). 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, do not use, stop use and ask a doctor if:, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol 80%

Purpose

Antiseptic

Uses

  • For handwashing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings

For external use only.
Flammable, keep away from fire or flame.

Do Not Use

in the eyes

Stop Use And Ask A Doctor If:

  • irritation and redness develop
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children.

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

Directions

  • Wet hands thoroughly with product and allow to dry without wiping

Other Information

  • avoid temperatures over 110°F
  • may discolor certain fabrics
  • harmful to wood finishes and plastics

Inactive Ingredients

Aloe Vera, Carbomer, Fragrance, Glycerin, Tocopheryl Acetate, Triethanolamine, Water

Questions?

Call 1 - 877 - 874 - 0606 Weekdays, 9AM – 5PM EST

Package Labeling:

Label2 (Label2)

Label2 (Label2)

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