Zuska
FDA Label NDC 53135-833

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 53135-833). 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, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, otc - questions, inactive ingredient, 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

Indications & Usage

Use: reduces underarm perspiration

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

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Dosage & Administration

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

Package Label.Principal Display Panel

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Image Of Canister Label (Canister)

Image Of Canister Label (Canister)

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