Foaming Hand Soap
FDA Label NDC 83986-224

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Uplift Brands, Llc for the product Foaming Hand (NDC 83986-224). 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, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When Using This Product

avoid contact with eyes. If contact occurs, rinse eyes with water.

Stop Use And Ask A Doctor If

  • irritation or redness develop
  • condition persists for more than 72 hours

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • wet hands 
  • apply palmful to hands 
  • scrub thoroughly 
  • rinse thoroughly

Inactive Ingredients

water, cocamidopropyl betaine, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, glycerin, citric acid, tetrasodium EDTA, sodium benzoate

Adverse Event

Manufactured By: Vi-Jon, Inc.

St. Louis, Mo 63114

Principal Display Panel

germ-X

Professional

ANTIBACTERIAL

FOAMING

HAND SOAP

1000 ML (33.8 FL OZ)

Image Description (Mm01)

Image Description (Mm01)

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