Suave Essentials Ocean Breeze Hand Sanitizer - Ethyl Alcohol Gel
Suave Skin Solutions Hand Sanitizer Lotion
Suave
FDA Label NDC 64942-2043
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 64942-2043). 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 essentials ocean breeze hand sanitizer - ethyl alcohol gel, 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 75.60%
Purpose
Antiseptic
Uses
helps decrease bacteria on the hands
Warnings
For external use only
Flammable. Keep away from fire or flame
Do not store in car.
Avoid contact with eyes,
In case of contact, rinse eyes thoroughly with water.
If irritation develops, 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 hand thoroughly with product and rub lightly until dry. Do not wipe off or rinse
Other Information
• May discolor fabrics or surfaces.
• Store below 105˚F (40˚C).
Inactive Ingredients
Water (Aqua), Glycerin, Fragrance (Parfum), Hydroxypropylcellulose, Lauryl Lactate, Myristyl Lactate, Cetyl Lactate, Cocos Nucifera (Coconut) Oil, Aloe Barbadensis Leaf Juice, Blue 1 (CI 42090) Red 33 (CI 17200).
Call
1-800-782-8301 or visit www.suave.com
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