Algoar Hand Sanitizer
FDA Label NDC 78884-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Grupo Algoar De Mexico, S.a. De C.v. for the product Algoar Hand Sanitizer (NDC 78884-001). 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, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 70% v/v.

Purpose

Antiseptic

Uses

For hand sanitizing

Warnings

For external use only. Flammable. Keep away from heat or flame.

When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water. Do not inhale or ingest.
Stop use and ask a doctor if irritation develop.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center.

Directions

  • Wet hands thoroughly with product and allow to dry without wiping.
  • For children under 6 use only under adult supervision.

Other Information

  • Do not store above 40C (104F). Store in a dry place.

Inactive Ingredients

Water, Glycerin, Carbomer,  Aloe vera, Triethanolamine, sucrose octaacetate

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