Everwipe Hand Sanitizer
FDA Label NDC 50157-518

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Brands International for the product Everwipe Hand Sanitizer (NDC 50157-518). 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 other, active ingredient, indications & usage, purpose, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

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Drug Facts

Active Ingredient

Ethyl Alcohol, 70% v/v

Indications & Usage

Antiseptic skin cleanser

Purpose

Antiseptic (skin) cleanser

Warnings

For external use only. Flammable, keep away from fire or flame.

Otc - When Using

When using this product.

  • If contact occurs, rinse thoroughly with water.
  • avoid contact with eyes.

Otc - Stop Use

Stop use and ask a doctor if irritation  develops.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • place enough product on your plam to thoroughly cover your hands
  • rub thoroughly into hands for at least 30 seconds
  • Allow to dry

Other Information

  • Store below 43°C (110°F)
  • may discolor certain fabrics or surfaces.

Inactive Ingredients

Carbomer, Aloe Barbadensis Leaf Extract, Aminomethyl Propanol, Glycerin, Propylene glycol, Water, Tocopheryl Acetate (Vit E).

Isopropyl Alcohol

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