Solgreat Alcohol-free Foaming Hand Sanitizer
FDA Label NDC 73913-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Panatural Usa, Inc. for the product Solgreat Alcohol-free Foaming Hand Sanitizer (NDC 73913-002). 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 active lngredient, purpose, uses, warnings, directions, inactive ingredients, keep out of reach of children., other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Lngredient

Benzalkonium Chloride

Purpose

Antibacterial

Uses

  • hand sanitizer to help reduce bacteria on the skin that could cause disease.
  • recommended for repeated use.

Warnings

For external use only.

When using this product, do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water,

Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Directions

  • place enough product in your palm to thoroughly cover your hands.
  • rub hands together until dry.
  • children under 6 years of age should be supervised when using this product.

Inactive Ingredients

cetrimonium chloride citric acid, cocamidopropyl betaine, cocamidopropylamine oxide, glycerin, propylene glycol, tocopheryl acetate, water.

Keep Out Of Reach Of Children.


Children must be supervised in use of this product.

Other Information

To prevent discoloration, avoid contact with clothing.

Product Label - 60 Ml Solgreat Alcohol-Free Hand Sanitizer Spray

60ml (Spray)

60ml (Spray)

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