Studio 35 Beauty
FDA Label NDC 0363-2013

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Company for the product Studio 35 Beauty (NDC 0363-2013). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredients: Aluminum Zirconium Trichlorohydrex Gly 20% (anhydrous)

Otc - Purpose

Purpose: Antiperspirant

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.

Indications & Usage

Use

  • Reduces underarm wetness
  • Extra effective

Warnings

Warning:

For external use only.

Do not use on broken skin.

Ask doctor before you use if you have kidney disease.

Stop use if rash or irritation occurs.

Dosage & Administration

Directions:

To dispense the proper dosage, turn the wheel one unit so the smooth or ribbed section is facing to the outside.Apply to underarms only.

Inactive Ingredient

Ingredients:Cyclopentasiloxane, Dimethicone crosspolymer, Hydrogenated Castor Oil, Talc, Dimethicone, Polyethylene, Fragrance

Package Label.Principal Display Panel

Label Front (Studiofront)

Label Front (Studiofront)

Label Back (Studioback)

Label Back (Studioback)

Studio (Studio)

Studio (Studio)

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