Prevail
FDA Label NDC 24488-021

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Duane Reade for the product Prevail (NDC 24488-021). 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, warnings, when using this product, otc - stop use, keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 62%.................................Antiseptic

Purpose

  • To decrease bacteria on the skin that could cause disease.
  • Recommended for repeated use.

Warnings

For external use only. Flammable. Keep away from heat and flame.

When Using This Product

  • Keep out of eyes. In case of contact with eyes, flush throughly with water
  • Avoid contact with broken skin.

Otc - Stop Use

If skin irritation develops.

Keep Out Of Reach Of Children

In case of accidental ingestion, seek professional assistance or contact Poison Control Center immediately.

Directions

  • Apply small amount to your palm, rub hands together throughly to coat, continue until hands are dry.

Other Information

  • Do not store above 105oF
  • May discolor some fabrics
  • Harmful to wood finishes and plastics

Inactive Ingredient

Water, Propylene Glycol, Glycerin, Carbomer, Isopropyl Myristate, Tocopheryl (Vitamin E) Acetate, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Yellow 5, Fragrance

Questions

Call (866) 375-6925

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