Hand Wash Soap
FDA Label NDC 69790-466

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Uline for the product Hand Wash (NDC 69790-466). 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 thoroughly with water.

Stop Use And Ask A Doctor If

  • irritation or redness develops
  • 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, glycerin, lauramine oxide, cocamidopropyl betaine, Aloe barbadensis leaf juice, PEG-150 distearate, cocamide MEA, fragrance, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4 yellow 5, red 4

Adverse Reactions

Distributed by Harmon Stores, Inc

650 Liberty Ave Union, NJ 07083 USA

Harmon Stores, Inc.

Visit us at www.facevalues.com

REFILL ONLY WITH FOAMING HAND SOAP, REGULAR LIQUID HAND SOAP WILL NOT FOAM.

Package Lable

ULINE

ANTIBACTERIAL

HAND SOAP

S-20662

7.5 FL OZ ( 221 mL)

Image Description (Mm3)

Image Description (Mm3)

* Please review the disclaimer below.