Duradry Am
FDA Label NDC 69990-200

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Novadore Usa, Llc for the product Duradry Am (NDC 69990-200). 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, uses, warnings, do not use, ask a doctor before use, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Aluminum Zirconium Trichlorohydrex Glycine 20%

Purpose

Antiperspirant

Uses

Reduces underarm perspiration

Warnings

For external use only
Stop use if rash or irritation occurs.

Do Not Use

  • On broken skin.

Ask A Doctor Before Use

if you have kidney disease

Keep Out Of Reach Of Children

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

Directions

  • Apply to underarms only.

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, C12-15 Alkyl Benzoate, Hydrogenated Castor Oil, Dimethicone, Zinc Ricinoleate, Petrolatum, Aluminum Starch Octenylsuccinate Fragrance.

Questions?

Visit us at www.duradry.com/am

Designed & developed by:
NOVADORE USA, INC
Miami, FL

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