Sure Fresh Essence
FDA Label NDC 41595-5421

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Idelle Labs, Ltd for the product Sure Fresh Essence (NDC 41595-5421). 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 front panel display, active ingredient, purpose, use, warnings, do not use, ask a doctor, stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Front Panel Display

Dry ProtectionSure Fresh EssenceAnti-Perspirant and Deodorant

Active Ingredient

Aluminum Zirconium Trichlorohydrex GLY 19% (anhydrous)

Purpose

Antiperspirant

Use

reduces underarm wetness

Warnings

For external use only.

Do Not Use

on broken skin

Ask A Doctor

before use if you have kidney disease

Stop Use

if rash or irritation occurs

Keep Out Of Reach Of Children.

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

Directions

apply to underarms only

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, Dimethicone, Petrolatum, PPG-14 Butyl Ether, Hydrogenated Castor Oil, Talc, Fragrance, Mineral Oil, Behenyl Alcohol

Questions?

1-800-487-7273
www.suredeodorant.com

Idelle Labs, Ltd.  All rights reserved.
Made in Canada and distributed by Idelle Labs, Ltd., El Paso, TX 79912
Sure® is a registered trademark of Helen of Troy Limited

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