Soft And Dri Clear Glide Is Antiperspirant Floral Bouquet
FDA Label NDC 54340-482

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Dial Corporation for the product Soft And Dri Clear Glide Is Antiperspirant Floral Bouquet (NDC 54340-482). 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 otc - active ingredient, otc - purpose, warnings, otc - do not use, otc - stop use, otc - keep out of reach of children, otc - ask doctor, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Aluminum Zirconium Pentachlorohydrex Gly 13.0%

Otc - Purpose

Antiperspirant

Use......reduces underarm perspiration

Warnings

Warning...For external use only

Otc - Do Not Use

Do not use on broken skin

Otc - Stop Use

Stop use and ask a doctor if rash or irritation occurs.

Otc - Keep Out Of Reach Of Children

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

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease.

Inactive Ingredient

Inactive Ingredients: cyclomethicone, Stearyl alcohol, PPG-14 butyl ether, hydrogenated castor oil, myristyl myristate, silica dimethyl silylate, C20-40 pareth-10, fragrance, red 40 lake.

How Supplied

The distinctive design and elements of this package are proprietary and owned by The Dial Corporation, A Henkel Company.

2010 Distributed by The Dial Corporation, A Henkel Company, Scottsdale, AZ, 85255. MADE IN CANADA

Dosage & Administration

Directions: Apply to underarms only

Indications & Usage

Use: reduces underarm perspiration.

* Please review the disclaimer below.