FDA.reportPublic FDA data

Zogics Antibacterial Foaming Hand

Manufacturer
Zogics, LLC
Effective date
2025-07-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 20:35:28

Label at a glance#

ProductZogics Antibacterial Foaming Hand
Active ingredientCHLOROXYLENOL
Label structure9 sections

Indications and uses

• Handwash to help decrease bacteria on the skin.

Dosage and administration

• Apply a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly. • Children under 6 years of age should be supervised when using this product.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.1%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic Handwashing

USES

INDICATIONS & USAGE SECTION

• Handwash to help decrease bacteria on the skin.

WARNINGS

WARNINGS SECTION

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

OTC - ASK DOCTOR 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 swallowed, get medical help or contact a Poison Control Center right away.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

• Apply a small amount of product to wet hands, work into lather for 30 seconds, and rinse thoroughly.
• Children under 6 years of age should be supervised when using this product.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water (Aqua) (7732-18-5), Sodium C14-16 Olefin Sulfonate (68439-57-6), Glycerin (56-81-5), Cocamidopropyl Hydroxysultaine (68139-30-0), Propanediol (26264-14-2), Propylene Glycol (57-55-6), Sodium Polyitaconate (26099-89-8), Dibromocyanoacetamide (10222-01-2), 2-Bromo-2-Nitropropane-1,3-Diol (52-51-7), Methylisothiazolinone (2682-20-4), Methylchloroisothiazolinone (26172-55-4)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display PanelPrincipal Display Panel

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72202-20172202-201-41

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
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
SODIUM POLYITACONATE (2800 MW, PHOSPHATE TERMINATED)G7SW5QN7TTIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PROPANEDIOL5965N8W85TIACT
BRONOPOL6PU1E16C9WIACT
GLYCERINPDC6A3C0OXIACT
DIBROMOCYANOACETAMIDE7N51QGL6MJIACT
CHLOROXYLENOL0F32U78V2QACTIB
METHYLISOTHIAZOLINONE229D0E1QFAIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
WATER059QF0KO0RIACT

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
3b00a75f-6a2a-5259-e063-6394a90af1ff13a4fd19-648c-88d8-e063-6294a90a03702025-07-28WarningsExact identifier
spl id: 3b00a75f-6a2a-5259-e063-6394a90af1ff
spl set id: 13a4fd19-648c-88d8-e063-6294a90a0370

Reported adverse events (FAERS/openFDA)#

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