Dry Idea Advanced Dry-powder Fresh
FDA Label NDC 54340-005

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 Dry Idea Advanced Dry-powder Fresh (NDC 54340-005). 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, otc - ask doctor, dosage & administration, 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  Ingredient Purpose

Aluminum Zirconium Pentacholrohydrex Gly 16.3%.......Antiperspirant

Otc - Purpose

Antiperspirant

Indications & Usage

Use

  • Reduces underarm perspiration
  • Extra effective


Warnings

Warnings for external use only.

Do not use on broken skin.

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.

Dosage & Administration

Directions Shake well. Apply to underarms only.

Inactive Ingredient

Inactive Ingredients: Cyclomethicone, Disteardimonium Hectorite, Propylene Carbonate, Gossypium Herbaceum(Cotton) Seed oil,Tocopheryl Acetate ( Vitamin E Acetate),Isopropyl Myristate, Fragrance,Zea Mays(Corn) Starch.

Otc - Questions

Questions? 1-800-258-DIAL

Package Label.Principal Display Panel

Dryidea-powderfresh.jpg

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