Belli Moisturizing Hand Sanitizer
FDA Label NDC 42281-101

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Abt Belli-materna Inc for the product Belli Moisturizing Hand Sanitizer (NDC 42281-101). 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 ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, 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

Active Ingredient

BENZALKONIUM CHLORIDE 0.1%

Purpose

ANTIMICROBIAL

Uses

  • REDUCES BACTERIA ON THE SKIN

Warnings

WHEN USING THIS PRODUCT

  • KEEP OUT OF EYES / RINSE WITH WATER TO REMOVE

    • STOP USE AND ASK A DOCTOR IF

    • RASH OR SKIN ORRITATION DEVELOPS

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN.

IN CASE OF ACCIDENTAL INGESTION, CONTACT A POISON CONTROL CENTER IMMEDIATELY.

Directions

  • PLACE ENOUGH PRODUCT IN YOUR HANDS TO THOROUGHLY COVER YOUR HANDS AND RUB IN.

Inactive Ingredients

WATER, SD ALCOHOL 40-B, POLYSORBATE 20, PEG-7 GLYCERYL COCOATE, ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER, TRIETHANOLAMINE, CITRUS LIMON (LEMON) PEEL OIL

* Please review the disclaimer below.