FDA.reportPublic FDA data

Oppeal. Hosmall Antibacterial Wipes

Manufacturer
Jiangsu Oppeal Daily Cosmetics Corp. Ltd.
Effective date
2020-08-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:18:31

Label at a glance#

ProductOppeal. Hosmall Antibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand sanitizing to help decrease bacteria on the skin

Dosage and administration

Tear off the sachet and use as required.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%(W/V)

Purpose

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

For hand sanitizing to help decrease bacteria on the skin

CAUTIONS

WARNINGS SECTION

  1. For external use only. Avoid contact with eyes or mouth. If contact occurs, rinse eyes thoroughly with warm water. 

Do not use 

OTC - DO NOT USE SECTION

on broken skin.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or redness occurs.

  • Store in a cool, dry place. Avoid heat or direct sunlight.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Do not flush. Dispose in a trash receptacle.

* Effective at killing 99.9% of germs as Canidia Albicans, Staphylococcus aureus and E.coli in the report Issued by the 3rd party

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Tear off the sachet and use as required.

OTHER INFORMATION

SPL UNCLASSIFIED SECTION

Store in a cool, dry place. Avoid heat or direct sunlight.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Aqua(Water), Glycerin, Propylene Glycol, Tocopherol Acetate, Aloe barbadensis Leaf Extract, 1,3-Butylene Glycol, PEG-7 Glyceryl Cocoate, Potassium Sorbate.

Package Labeling:1ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Package Labeling:5ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling:10ct

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77828-00577828-005-01, 77828-005-05, 77828-005-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALOE VERA LEAFZY81Z83H0XIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
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
d4ae78cc-e364-1a97-e053-2a95a90a5922acc65b1e-eeaa-87c5-e053-2995a90af2052022-01-03WarningsExact identifier
spl set id: acc65b1e-eeaa-87c5-e053-2995a90af205

Reported adverse events (FAERS/openFDA)#

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