Nordland Hand Sanitizer
FDA Label NDC 90029-003

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nordland Development, S. De R.l. De C.v. for the product Nordland Hand Sanitizer (NDC 90029-003). 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, purpose, inactive ingredients, use(s), keep out of reach of children., warnings, do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredients

Ethyl Alcohol 70% v/v

Purpose

Antiseptic

Inactive Ingredients

Glycerin, distilled water, triethanolamine, carbomer and fragrance

Use(S)

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

  • 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 Ask A Doctor

if irritation or rush occurs. These may be signs of a seious condition.

Other Information

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

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

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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