Armicare Hand Sanitizer Liquid
FDA Label NDC 81793-187

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Armis Biopharma, Inc for the product Armicare Hand Sanitizer (NDC 81793-187). 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, do not use, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Ethyl Alcohol 75% v/v.

Purpose

Antiseptic

Uses

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

  • On 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 or rash occurs. These may be signs of a serious condition.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222

Directions:

  • 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.

Other Information:

  • Store between 15-30C (59-86F )
  • Avoid freezing and excessive heat above 40C (104F)

Inactive Ingredients:

Deionized water, Glycerin, Hydrogen Peroxide, Acetic Acid, Lavender, Polysorbate-20

Questions?

1-800-970-1779

Package Labeling:

Label (Label)

Label (Label)

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