Zuska
FDA Label NDC 53135-837

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Raani Corporation for the product Zuska (NDC 53135-837). 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, dosage & administration, otc - questions, inactive ingredient, otc - keep out of reach of children, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredients: Aluminum Zirconium Trichlorohydrex Gly (18%)

Otc - Purpose

Purpose: Antiperspirant


Warnings

Warnings: For external use only.  Do not use on broken skin.  Stop us if rash or irritation occurs.  Ask a doctor before use if you have kidney disease.  Stop use and ask a doctor if rash or irritation occurs.  Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions: Apply to underarms only

Inactive Ingredient

Inactive Ingredients: Cyclopentasiloxane, Stearyl alcohol, Hydrogenated Castor Oil, Dipropylene Glycol Dibenzoate, Fragrance, PEG-8 Distearate, Silica, Aluminum Strach Octenyl Succinate, Mineral Oil, Cocos Nucifera (Coconut) Oil, Aloe Barbadensis (Aloe Vera) Leaf Extract

Otc - Keep Out Of Reach Of Children


Indications & Usage

Use: reduces underarm perspiration

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