Dosage and administration
pump into dry hands lather vigorously for at least 30 seconds wash skin, rinse thoroughly and dry
HEB HEB5719269-00 149.000/149AA
- Manufacturer
- H E B
- Effective date
- 2026-07-15
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- daily-update
- Hydrated at
- 2026-07-18 05:11:27
Label at a glance#
ProductBenzalkonium Chloride
Active ingredientBENZALKONIUM CHLORIDE
Label structure14 sections
Contacts and useful links#
Label contents#
Full prescribing information#
Claims
Dermatologist Tested
pH Balanced
No Animal Testing
Moisturizing & Gentle on Hands
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 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
- pump into dry hands
- lather vigorously for at least 30 seconds
- wash skin, rinse thoroughly and dry
Inactive ingredients
Water, Glycerin, Lauramidopropylamine Oxide, Cetrimonium Chloride, Cocamidopropyl Betaine, Sodium Benzoate, Fragrance, Citric Acid, Aloe Barbadensis Leaf Juice, Sodium Chloride, Disodium EDTA, Benzophenone-4, Blue 1, Red 33
Questions or comments?
Call toll-free 1-800-370-5360
Disclaimer
*ENCOUNTERED IN HOUSEHOLD SETTINGS
Adverse Reactions
100% GUARANTEE promise
If you aren't completely pleased with this product, we'll be happy to replace it or refund your money. You have our word on it.
MADE WITH PRIDE AND CARE FOR H-E-B ®,
SAN ANTONIO, TX 78204
US ONLY
PLASTIC BOTTLE
Widely Recyclable
Empty Contents
how2recycle.info
Principal Display Panel
Kills 99% of Bacteria*
H-E-B ®
ANTIBACTERIAL FOAMING HAND WASH REFILL
SOOTHING SPRINGS SCENT
MADE WITHOUT
Sulfates, Parabens, Phthalates or Silicones
REFILL 32 OZ = 4 REFILLS
32 FL OZ (1QT) 946 mL
Products#
Every source-derived product name is available through these pages.
- Benzalkonium Chloride
- EDETATE DISODIUM
- COCAMIDOPROPYL BETAINE
- LAURAMIDOPROPYLAMINE OXIDE
- CETRIMONIUM CHLORIDE
- ALOE VERA LEAF JUICE
- SODIUM BENZOATE
- FD&C BLUE NO. 1
- CITRIC ACID
- WATER
- GLYCERIN
- D&C RED NO. 33
- SODIUM CHLORIDE
- SULISOBENZONE
- BENZALKONIUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 59640-149 | 59640-149-96, 59640-149-45 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| EDETATE DISODIUM | 7FLD91C86K | IACT |
| COCAMIDOPROPYL BETAINE | 5OCF3O11KX | IACT |
| LAURAMIDOPROPYLAMINE OXIDE | I6KX160QTV | IACT |
| CETRIMONIUM CHLORIDE | UC9PE95IBP | IACT |
| ALOE VERA LEAF JUICE | RUE8E6T4NB | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| CITRIC ACID | 2968PHW8QP | IACT |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| D&C RED NO. 33 | 9DBA0SBB0L | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SULISOBENZONE | 1W6L629B4K | IACT |
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Benzalkonium Chloride | BENZALKONIUM CHLORIDE | H E B | 56ab94e1-ef63-238a-e063-6394a90a5fdb | 2026-07-15 | Warnings, Adverse reactions | 59640-149-96 59640-149-45 59640-149 59640014945 59640014996 56ab94e1-ef64-238a-e063-6394a90a5fdb 56ab94e1-ef63-238a-e063-6394a90a5fdb |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.