Hand Sanitizer Gel
FDA Label NDC 67326-005

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Degasa, S.a. De C.v. for the product Hand Sanitizer (NDC 67326-005). 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, purpose, inactive ingredients, uses, when using this product, directions, other information, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Ethyl alcohol 70%

Purpose

Antiseptic

Inactive Ingredients

Deionized water, Carbopol, Glycerin, Triethanolamine, Aminomethylpropanol, Fragances.

Uses

To decrease bacteria on the skin that could disease. Recommended for repeated use.

When Using This Product

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.
Do not inhale or ingest.

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6, use only under adults supervision.
  • Not recommended for infants

Other Information

- Do not store above 105° F.
- Harmful to wood finishes and plastic.

Warnings

- For external use only: hands.
- Flammable, keep away from fire or flame.
- Keep out of reach of children.

Package Labeling:

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