Active Ingredient
Ethyl Alcohol 62%
Prevail
FDA Label NDC 24488-020
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 24488-020). 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, use, warnings, when using this product, stop use and ask doctor if, keep out of reach of children., other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
...............................Antiseptic
Use
- 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.
Stop Use And Ask Doctor If
If skin irritation develops.
Keep Out Of Reach Of Children.
In case of accidental ingestion, seek professional assistance or contact Poison Control Center immediately.
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, Red 33, Fragrance
Questions
Call (866) 375-6925
Directions
Apply small amount to your palm, rub hands together throughly to coat, continue until hands are dry.
Package Label.Principal Display Panel
Placeholder Text
Dr_prevail_handsani8oz_pom (Dr Prevail Handsani8oz Pom)
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