FDA.reportPublic FDA data

Antibacterial Wet Wipes

Manufacturer
TIANJIN YANSHENG INDUSTRIAL TRADE COMPANY
Effective date
2022-03-19
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:05:38

Label at a glance#

ProductAntibacterial Wet Wipes
Active ingredientBENZETHONIUM CHLORIDE
Label structure6 sections

Dosage and administration

For adults and children of 2 years and over use on hands and face to clean and refresh, allow skin to air dry. For children under 2 years ask a doctor before use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.115%

PURPOSE

OTC - PURPOSE SECTION

Antibacterial

Use

INDICATIONS & USAGE SECTION

decreases bacteria on skin

WARNINGS

WARNINGS SECTION

For external use only.
Do not use over large areas of the body if you are allergic to any of the ingredients.When using this product do not get into eyes.If contact occurs, rinse thoroughly with water.Stop use and ask a doctor if irritation or rash develops and ontinues for more than 72 hours.

Keep out of reach of children.

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

For adults and children of 2 years and over use
on hands and face to clean and refresh, allow
skin to air dry.
For children under 2 years ask a doctor before use.

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Water,SD Alcohol 40,Propylene Glycol,Aloe Barbadensis Leaf,Potassium sorbate,Tocopherol,Quaternium 52,PEG-60 Lanolin,Citric Acid,Disodium EDTA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70031-003-012022-03-19C16284748780-19d75b9cf-ec63-f424-e053-dadaa90a57ce70031-003 Antibacterial Wet Wipes
70031-003-022022-03-19C16284748780-19d75b9cf-ec63-f424-e053-dadaa90a57ce70031-003 Antibacterial Wet Wipes
70031-003-032022-03-19C16284748780-19d75b9cf-ec63-f424-e053-dadaa90a57ce70031-003 Antibacterial Wet Wipes
70031-003-042022-03-19C16284748780-19d75b9cf-ec63-f424-e053-dadaa90a57ce70031-003 Antibacterial Wet Wipes
70031-003-012020-01-31C16284748780-19d75b9cf-ec63-f424-e053-dadaa90a57ce70031-003 Antibacterial Wet Wipes
70031-003-022020-01-31C16284748780-19d75b9cf-ec63-f424-e053-dadaa90a57ce70031-003 Antibacterial Wet Wipes
70031-003-032020-01-31C16284748780-19d75b9cf-ec63-f424-e053-dadaa90a57ce70031-003 Antibacterial Wet Wipes
70031-003-042020-01-31C16284748780-19d75b9cf-ec63-f424-e053-dadaa90a57ce70031-003 Antibacterial Wet Wipes

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
70031-00370031-003-01, 70031-003-02, 70031-003-03, 70031-003-04

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
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT
QUATERNIUM-22MXO138JCBPIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DISODIUM EDTA-COPPER6V475AX06UIACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB
CITRACONIC ACID0RQ6CXO9KDIACT
ALCOHOL3K9958V90MIACT
TOCOPHEROLR0ZB2556P8IACT
ALOE VERA LEAFZY81Z83H0XIACT
PEG-60 CASTOR OILVXP26NM2XXIACT

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
da8daf04-fa21-2ea3-e053-2a95a90a27612db1d3d7-735b-61f3-e054-00144ff88e882022-03-19WarningsExact identifier
spl id: da8daf04-fa21-2ea3-e053-2a95a90a2761
spl set id: 2db1d3d7-735b-61f3-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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