Suave Hand Sanitizer Professional
FDA Label NDC 50069-109

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Unilever Asia Private Limited for the product Suave Hand Sanitizer Professional (NDC 50069-109). 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, use, warnings, keep out of reach of children., otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Alcohol (75% v/v)

Purpose

ANTISEPTIC

Use

Help decrease bacteria on the hands

Warnings

For external use only.

Flammable, Keep away from heat or flame.

Avoid contact with eyes, in case of contact, rinse eyes thoroughly with water immediately.

If irritation develops, discontinue use and consult a doctor.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children except under adult supervision. If swallowed, get medical help or contact a poison control center right away.

Directions

  • Wet hands thoroughly with product and rub lightly until dry. Do not wipe off or rinse.

Other Information

  • May discolor fabrics or surfaces. Store below 95°F (35°C).

Inactive Ingredients

Carbomer, Denatonium Benzoate, Purified Water USP, Tert-butyl Alcohol, Triethanolamine.

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