FDA.reportPublic FDA data

Antibacterial Foaming Hand Wash

Manufacturer
Sonchin Biomedical Cosmetics CORP.
Effective date
2021-07-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:39:28

Label at a glance#

ProductAntibacterial Foaming Hand Wash
Active ingredientBENZALKONIUM CHLORIDE
Label structure10 sections

Dosage and administration

Wash hands and rinse Supervise children under 6 years of age when using this product to avoid swallowing Other information Store between 20°C~25°C (68°F~77°F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

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. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Irritation or 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

  • Wash hands and rinse
  • Supervise children under 6 years of age when using this product to avoid swallowing

Other information

  • Store between 20°C~25°C (68°F~77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Cocamidopropyl Betaine, Cocamide DEA, Decyl Glucoside, Glycerin, Lauramidopropylamine Oxide, Myristamidopropylamine Oxide, Polysorbate 20, Aloe Barbadensis Leaf Juice, Fragrance, Tetrasodium EDTA, Citric Acid, Methylchloroisothiazolinone, Methylisothiazolinone.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

025-01025-01259 mL NDC: 73662-025-01

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
73662-02573662-025-01

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
MYRISTAMIDOPROPYLAMINE OXIDE3HSF539C9TIACT
DITETRACYCLINE TETRASODIUM EDETATEWX0A0IT7K5IACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
GLYCERINPDC6A3C0OXIACT
COCO DIETHANOLAMIDE92005F972DIACT
ALOE VERA LEAFZY81Z83H0XIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
LAUROYL/MYRISTOYL AMIDOPROPYL AMINE OXIDEHY9O6ZW9CYIACT
POLYSORBATE 207T1F30V5YHIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
CITRIC ACID ACETATEDSO12WL7AUIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
e14f380e-959f-9161-e053-2a95a90a8a3ac83bd9cc-4da1-2836-e053-2a95a90a04652022-06-13WarningsExact identifier
spl set id: c83bd9cc-4da1-2836-e053-2a95a90a0465

Reported adverse events (FAERS/openFDA)#

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