Suave Hand Sanitizer Spray - Ethyl Alcohol Liquid
Suave Hand Sanitizer Spray
Suave
FDA Label NDC 64942-1739
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Conopco Inc. D/b/a/ Unilever for the product Suave (NDC 64942-1739). 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 suave hand sanitizer spray - ethyl alcohol liquid, drug facts, purpose, uses, warnings, 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
Drug Facts
Active ingredient
Ethyl Alcohol (72%)
Purpose
Antiseptic
Uses
help decrease bacteria on the hands
Warnings
• For external use only
• Flammable. Keep away from fire or flame
• Avoid contact with eyes,
in case of contact, rinse eyes thoroughly with water immediately.
• If irritation develps, discontinue use and consult a doctor.
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 allow to dry without wiping. Rub lightly until dry. Do not rinse.
Other Information
May discolor fabrics or surfaces. Store below 105˚F (40˚C).
Inactive Ingredients
Glycerin, Water (Aqua).
Questions?
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