FDA.reportPublic FDA data

Zep Handstand Antimicrobial

Manufacturer
Zep Inc. | Kutol Products Company
Effective date
2020-11-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:06:37

Label at a glance#

ProductZep Handstand Antimicrobial
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

Handwash to help decrease bacteris on the skin.

Dosage and administration

Apply a small amount, covering hands with product for 30 seconds. Add water, lather and rinse. Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Antibacterial handwashing

Uses

INDICATIONS & USAGE SECTION

Handwash to help decrease bacteris on the skin.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use in the eyes. In case of eye contact, immediately flush with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallow, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply a small amount, covering hands with product for 30 seconds. Add water, lather and rinse.
  • Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENT SECTION

Water, Cetrimonium Chloride, Sodium Chloride, Lauramine Oxide, Sorbitol, Disodium EDTA, Cocamide MEA, PEG-120 Methyl Glucose Dioleate, Sodium Lauriminodipropionate, Citric Acid, Fragrance, Methylisothiazolinone, Methylchloroisothiazolinone, Yellow 5, Red 33

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

U429U429

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66949-42966949-429-01

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
SODIUM LAURIMINODIPROPIONATE7G447D0DH9IACT
LAURAMINE OXIDE4F6FC4MI8WIACT
SORBITOL506T60A25RIACT
COCO MONOETHANOLAMIDEC80684146DIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
D&C RED NO. 339DBA0SBB0LIACT
WATER059QF0KO0RIACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
SODIUM CHLORIDE451W47IQ8XIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
METHYLISOTHIAZOLINONE229D0E1QFAIACT

Source Document#

Source XML · Source PDF

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
b464669e-c3a8-6a52-e053-2a95a90abd085cc4c45d-5b71-0912-e053-2991aa0a10a52020-11-18WarningsExact identifier
spl id: b464669e-c3a8-6a52-e053-2a95a90abd08
spl set id: 5cc4c45d-5b71-0912-e053-2991aa0a10a5

Reported adverse events (FAERS/openFDA)#

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