Vanilla Hand Sanitizer
FDA Label NDC 54860-089

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Lantern Science Co., Ltd. for the product Vanilla Hand Sanitizer (NDC 54860-089). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, warnings, dosage & administration, inactive ingredient, indications & usage, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredient

Benzalkonium Chloride 0.1%

Otc - Purpose

Antibacterial

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Warnings

Warnings

  • for external use only
  • if irritation occurs discontinue use
  • keep out of eyes
  • avoid contact with broken skin
  • do not inhale or ingest
  • stop use and ask if doctor if skin irritation develops
  • keep out of reach of children
  • if swallowed, get medical help or contact a poison control center right away.

Dosage & Administration

Directions

  • Rub a dime sized drop into hands.
  • For children under 6 use under adult supervision.

Inactive Ingredient

Inactive Ingredients

water/aqua, hydroxyethylcellulose, phenoxyethanol, fragrance/parfum, disodium edta

Package Label.Principal Display Panel

Label (Tb01905)

Label (Tb01905)

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