Mentholatum Moisturizing Hand Sanitizer Gel
FDA Label NDC 10742-0004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by The Mentholatum Company for the product Mentholatum Moisturizing Hand Sanitizer (NDC 10742-0004). 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 ingredients, purpose, uses, warnings, when using this product, stop use and ask a doctor if, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Benzalkonium Chloride 0.13%

Purpose

Skin antiseptic

Uses

  • Hand sanitizer to reduce bacteria on the skin

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

  • irritation or rash appears and lasts.

Directions

  • Liberally apply product in your palm to thoroughly cover your hands
  • Rub hands together briskly until absorbed.
  • Children under 6 years of age should be supervised when using this product.

Inactive Ingredients

purified water, hydroxypropyl starch phosphate, lauryl glucoside, dimethicone, chlorphenesin, edetate disodium, glycerin, hyaluronic acid, methyl gluceth-20, phenoxyethanol, polyquaternium-7, rosmarinus officinalis (rosemary) leaf oil, silanetriol

Questions?

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