Dr. Rothmans Dermashield
FDA Label NDC 89153-796

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by High Desert Pharmaceutics, Inc. for the product Dr. Rothmans Dermashield (NDC 89153-796). 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 - keep out of reach of children, otc - purpose, otc - when using, warnings, otc - ask doctor, indications & usage, dosage & administration, 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

  • Ethyl Alcohol - 62%
  • Benzalkonium Chloride - 0.10%

Otc - Keep Out Of Reach Of Children

Warning

  • Keep out of reach of children.

Otc - Purpose

Purpose

  • Antiseptic
  • Antibacterial

Otc - When Using

Directions

  • Apply by spraying and gently spreading onto skin.

Warnings

Warning  

  • For external use only.
  • Flammable keep away from fire or flame
  • Do not use in eyes. In case of contact, rinse eyes thoroughly with water.

Otc - Ask Doctor

Warning

  • Stop use and ask doctor if irritation and redness persist for more than 72 hours.

Indications & Usage

Sanitizer and moisturizer

Dosage & Administration

Apply by spraying and gently spreading onto skin

Inactive Ingredient

Blended Silicone Polyethers

Package Label.Principal Display Panel

Dr Rothman's Dermashield

Image Of Bottle Label (Dermashield)

Image Of Bottle Label (Dermashield)

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