Utrasure
FDA Label NDC 61924-266

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dermarite Industries Llc for the product Utrasure (NDC 61924-266). 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:, directions:, other information, inactive ingredients:, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Aluminum Sesquichlorohydrate 15%

Purpose:

Anti-perspirant

Uses:

  • Reduce underarm wetness
  • 24 hour protection

Warnings:

  • For external use only.
  • Do not use on broken skin.
  • Avoid contact with eyes. In case of contact, flush thoroughly with water.
  • Stop use and ask doctor if you have Kidney Disease.

    • Keep out of reach of children. If swallowed, contact physician or Poison Control Center right away.

Directions:

  • Apply to under arms only.
  • Hold in an upright position about 6 inches from the underarm and spray.

Other Information

  • Store at room temperature (59°-86°F).
  • You may report a serious adverse event to DermaRite Industries, PO Box 7209, North Bergen, NJ 07047

Inactive Ingredients:

Fragrance, PEG-40 Castor Oil, Propylene Glycol, SD Alcohol 40-B, Water

Questions?

Call 1-800-337-6296 Mon-Fri 9AM-5PM EST.

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