FDA.reportPublic FDA data

Hand Wash

Manufacturer
Permatex | Consumer Product Partners, LLC
Effective date
2024-09-18
Label type
HUMAN OTC DRUG LABEL
Version
12
Source
legacy-cache
Hydrated at
2026-08-01 20:54:47

Label at a glance#

ProductHand Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Dosage and administration

apply palmful to dry hands scrub thoroughly rinse thoroughly

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 develops
  • 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

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, glycerin, lauramine oxide, cocamidopropyl betaine, PEG-150 distearate, cocamide MEA, fragrance, citric acid, tetrasodium EDTA, DMDM hydantoin, benzophenone-4, blue 1, red 33

adverse reaction

SPL UNCLASSIFIED SECTION

PERMATEX and design are TMs of Illinois Tool Works, Inc. 2016 Permatex, a division of ITW.

Solon, OH 44139/  Assembled in U.S.A. with U.S. and global materials

www.permatex. com Item # 95105

743.000/743AA

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FAST ORANGE

Antibacterial FOAMING HAND WASH

FRESH SCENT!

Helps kill harmful germs

Gentle enough for everyday use

7.5 FL OZ (221 mL)

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70616-74370616-743-96

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
LAURAMINE OXIDE4F6FC4MI8WIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PEG-150 DISTEARATE6F36Q0I0ACIACT
COCO MONOETHANOLAMIDEC80684146DIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
EDETATE SODIUMMP1J8420LUIACT
DMDM HYDANTOINBYR0546TOWIACT
SULISOBENZONE1W6L629B4KIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
2eabfab2-eeb6-6d9c-e063-6294a90a5a7ade8bd82e-7449-4eac-ba8c-6b02be27024d2025-02-21WarningsExact identifier
spl set id: de8bd82e-7449-4eac-ba8c-6b02be27024d

Reported adverse events (FAERS/openFDA)#

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