FDA.reportPublic FDA data

Done Hand Antibacterial Fruity Fusion

Manufacturer
Olein Recovery Corporation
Effective date
2021-03-04
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:49:35

Label at a glance#

ProductDone Hand Antibacterial Fruity Fusion
Active ingredientBENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

wash skin, rinse and dry 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 ths skin.

Warnings

WARNINGS SECTION

For external use only

When using this product,

OTC - WHEN USING SECTION

avoid contact with eyes. In case of contact flush with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

wash skin, rinse and dry thoroughly

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water, sodium laureth sulfate, sodium C14-16 olefin sulfonate, cocamidorpyopyl betaine, sodium chloride, glycerine, fragrance, tetrasodium EDTA, methylchloroisothiazolinone, Methylisothiazolinone, D&C orange No.4

Package Labeling: Done Hand Soap Antibacterial Fruity Fusion, 296,mL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

123123

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
77142-00977142-009-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM LAURETH SULFATEBPV390UAP0IACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
SODIUM CHLORIDE451W47IQ8XIACT
GLYCERINPDC6A3C0OXIACT
EDETATE SODIUMMP1J8420LUIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
D&C ORANGE NO. 4Q1LIY3BO0UIACT
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
ebda4763-c4bc-ea20-e053-2a95a90a7069a560ab0e-af7c-c78c-e053-2995a90aedad2022-10-25WarningsExact identifier
spl set id: a560ab0e-af7c-c78c-e053-2995a90aedad

Reported adverse events (FAERS/openFDA)#

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