Scent-a-way Odor Control Max
FDA Label NDC 10889-418

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Vvf Kansas Services Llc for the product Scent-a-way Odor Control Max (NDC 10889-418). 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, otc - do not use, otc - ask doctor, otc - stop use, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Aluminum Zirconium Trichlorohydrex GLY 20%

Purpose

Anti-perspirant

Use

Reduces underarm wetness.

Warnings

For external use only.

Otc - Do Not Use

Do not use on broken skin.

Otc - Ask Doctor

Ask a doctor before use if you have kidney disease.

Otc - Stop Use

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:

Turn dial to raise product.  Apply to underarm only.

Other Information:

Avoid storage at extreme temperatures (below 35°F and above 115°F).

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, Mineral Oil, Hydrogenated Castor Oil, Cetyl

Alcohol, Diisopropyl Adipate, Aluminum Starch, Octenylsuccinate, Glyceryl

Stearate, PEG-100 Stearate, Silver Citrate, Silica, Zinc Ricinoleate, PPG-14 Butyl

Ether, Water, Citric Acid, Talc.

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