Myremede Hand Sanitizer
FDA Label NDC 77529-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Remede Organics, Inc. for the product Myremede Hand Sanitizer (NDC 77529-000). 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 ingredients[s], purpose, uses[s], warnings, do not use:, when using this product, stop use and consult a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredients[S]

Alcohol 75% v/v

Purpose

Antiseptic

Uses[S]

Hand sanitizer to help reduse bacteria that potentially can cause disease. For use when stop and water are not available.

Warnings

For external use only. Flammable.

Keep away from heat or flame.

Do Not Use:

  • in 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 Consult 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.

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until  dyr.
  • 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

aqua (water), glycerin, carbomer, propylene glycol, sodium hydroxide, parfum (fragrance), aloe barbadensis leaf extract

Package Labeling 100 Ml

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Package Labeling 280Ml

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Package Labeling 500Ml

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Package Labeling 2000Ml

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