FDA.reportPublic FDA data

HEB HEB5719266-00 346

Manufacturer
H E B
Effective date
2026-07-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-18 05:11:06

Label at a glance#

ProductBenzalkonium Chloride
Active ingredientBENZALKONIUM CHLORIDE
Label structure14 sections

Dosage and administration

pump into dry hands lather vigorously for at least 30 seconds wash skin, rinse thoroughly and dry

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

BENZALKONIUM CHLORIDE 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

for handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only: hands only

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • pump into dry hands
  • lather vigorously for at least 30 seconds
  • wash skin, rinse thoroughly and dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Lauramidopropylamine Oxide, Cetrimonium Chloride, Cocamidopropyl Betaine, Sodium Bezoate, Fragrance, Citric Acid, Aloe Barbadensis Leaf Juice, Sodium Chloride, Disodium EDTA, Green 5, Red 33, Yellow 5, Yellow 6

Questions or comments?

OTC - QUESTIONS SECTION

Call toll-free 1-800-370-5360

Disclaimer

SPL UNCLASSIFIED SECTION

*ENCOUNTERED IN HOUSEHOLD SETTINGS

Adverse Reactions

ADVERSE REACTIONS SECTION

MADE WITH PRIDE AND CARE FOR H-E-B ®,

SAN ANTONIO, TX 78204

US ONLY

PLASTIC BOTTLE

Widely Recyclable

Empty Contents

how2recycle.info

Claims

SPL UNCLASSIFIED SECTION

Dermatologist Tested

pH Balanced

No Animal Testing

Moisturizing & Gentle on Hands

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Kills 99% of Bacteria*

H-E-B ®

ANTIBACTERIAL FOAMING HAND WASH

COCONUT VANILLA SCENT

MADE WITHOUT

Sulfates, Parabens, Phthalates or Silicones

7.5 FL OZ (221 mL)

mm01mm01mm02mm02

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
59640-34659640-346-96

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
D&C GREEN NO. 58J6RDU8L9XIACT
FD&C YELLOW NO. 6H77VEI93A8IACT
D&C RED NO. 339DBA0SBB0LIACT
LAURAMIDOPROPYLAMINE OXIDEI6KX160QTVIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
SODIUM CHLORIDE451W47IQ8XIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
GLYCERINPDC6A3C0OXIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE DISODIUM7FLD91C86KIACT
ALOE VERA LEAF JUICERUE8E6T4NBIACT
SODIUM BENZOATEOJ245FE5EUIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Benzalkonium ChlorideBENZALKONIUM CHLORIDEH E B56426ecd-e3e7-46df-e063-6394a90ab5cd2026-07-10Warnings, Adverse reactionsExact identifier
ndc (package): 59640-346-96
ndc (product): 59640-346
ndc11 (package): 59640034696
spl id: 56426ecd-e3e8-46df-e063-6394a90ab5cd
spl set id: 56426ecd-e3e7-46df-e063-6394a90ab5cd

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.