FDA.reportPublic FDA data

Antibacterial Handsoap

Manufacturer
BLUE CROSS LABORATORIES
Effective date
2020-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:19:07

Label at a glance#

ProductAntibacterial Handsoap
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Indications and uses

For handwashing to decrease bacteria on the skin

Dosage and administration

wet hands as needed Lather vigorously for at least 15 seconds Wash skin, rinse and dry thoroughly

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%. Purpose: Antibacterial

Purpose

OTC - PURPOSE SECTION

Antibacterial, Hand soap

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • Avoid contact with eyes. In case of eye contact, flush with water

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation and redness develops.

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

  • wet hands as needed
  • Lather vigorously for at least 15 seconds
  • Wash skin, rinse and dry thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Sodlium Laureth Sulfate, Cocamidopropyl Betaine, Cocamide DIPA, Glycerin, Citric acid, Methylisothiazolinone, Fragrance, Sodium Chloride, FD&C Red 40, D&C Red 33, FD&C Yellow 5

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

355 mL NDC: 22431-152-01

PDPPDP

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
22431-15222431-152-01
75729-004

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
FD&C RED NO. 40WZB9127XOAIACT
GLYCERINPDC6A3C0OXIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM CHLORIDE451W47IQ8XIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
D&C RED NO. 339DBA0SBB0LIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
COCO DIISOPROPANOLAMIDES485AM948QIACT
FD&C YELLOW NO. 5I753WB2F1MIACT

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
c439c202-17d3-45f8-e053-2995a90a284dac3dded2-79f7-628a-e053-2a95a90af18c2021-06-07WarningsExact identifier
spl set id: ac3dded2-79f7-628a-e053-2a95a90af18c

Reported adverse events (FAERS/openFDA)#

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