Vanilla Germ Killa Hand Sanitizer
FDA Label NDC 54860-080

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 Germ Killa Hand Sanitizer (NDC 54860-080). 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%

Purpose: Antibacterial

Otc - Purpose

Use

To decrease bacteria on the skin that could cause disease.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Warnings

Warnings

  • for external use only-hands.
  • keep out of eyes. avoid contact with broken skin.
  • stop use and ask a Doctor if irritation or redness develops.
  • do not inhale or ingest. 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/eau), glycerin, coceth-7, PPG-1-PEG-9 lauryl glycol ether, carbomer, hydrogenated castor oil, fragrance (parfum).

May Contain

Red 40 (CI 16035), Red 33 (CI 17200), Blue 1 (CI 42090), Yellow 5 (CI 19140).

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