Soapbox Hand Sanitizer
FDA Label NDC 75115-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Soapbox Soaps, Llc for the product Soapbox Hand Sanitizer (NDC 75115-002). 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 drug facts, active ingredient:, purpose, uses, warnings, do not use, when using this product,, discontinue use if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredient:

Ethyl Alcohol 70% v/v

Purpose

Antimicrobial

Uses

Hand sanitizer to help reduce bacteria on the skin

Warnings

For external use only. Flammable. Keep away from fire or flame.

Do Not Use

  • in children less than 2 months of age
  • on open skin wounds

When Using This Product,

keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Discontinue Use If

irritation or redness develops. If condition persists for more than 72 hours, consult a doctor.

Keep Out Of Reach Of Children.

If swallowed get medical help or call a poison control center immediately.

Directions

  • Place enough product in your palm to thoroughly cover your hands.
  • Rub hands together briskly untill dry.
  • Children under 6 years of age should be supervised when using this product.

Other Information:

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

Inactive Ingredients:

Water, Glycerin, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Citric Acid, Sodium Hydroxide

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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