Foaming Antibacterial Handsoap Liquid
FDA Label NDC 68041-512

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Chemcor Chemical Corporation for the product Foaming Antibacterial Handsoap (NDC 68041-512). 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 drug facts, active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Antibacterial

Uses

  • Antibacterial foaming hand cleaner.
  • Use in daycare, hospitals, nursing homes, physician offices, dental offices and clinics.

Warnings

  • For external use only.
  • Avoid contact with eyes.
  • If contact occurs, rinse thoroughly with water.
  • Discontinue use if irritation to redness develops.
  • If irritation persists for more than 72 hours, consult a physician.

Otc - Keep Out Of Reach Of Children

  • KEEP OUT OF REACH OF CHILDREN.
  • If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Read the entire label before using this product.
  • Ready to use without dilution.
  • Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands.
  • Rinse with clean water and dry.

Inactive Ingredients

Water, Decyl Glucoside, Glycerin, Fragrance, Methylisothiazolinone, Citric Acid, FD&C Yellow No. 5, Aloe Vera, Red Dye (FD&C)

Packaging

Image (6804151201)

Image (6804151201)

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