FDA.reportPublic FDA data

Wet Wipes Antibacterial Hand Wipes

Manufacturer
Ningbo Yinzhou GreenLight International Trade Co.,Ltd | NINGHAI WEIYI DAYLY NECESSITIES FACTORY | Ningbo Yinzhou Lvguang International Trade Co.,Ltd
Effective date
2020-05-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:59

Label at a glance#

ProductWet Wipes Antibacterial Hand Wipes
Active ingredientBENZETHONIUM CHLORIDE
Label structure7 sections

Dosage and administration

Directions Adults and children 2 years and over apply to hands allow to dry without wiping Children under 2 years ask a doctor before use

Storage and handling

Other information store at room temperature may discolor certain fabrics

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzethonium Chloride 0.3%

Purpose

OTC - PURPOSE SECTION

Purpose Antimicrobial

Use

INDICATIONS & USAGE SECTION

Use

Decrease bacteria on skin

Warnings

WARNINGS SECTION

For External use only

Do not use

OTC - DO NOT USE SECTION

Do not use if you are allergic to any of the ingredients

When using this product

SAFE HANDLING WARNING SECTION

​When using this product do not get into eyes, if contact occurs rinse thoughly with water

Stop use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues for more then 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

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

Adults and children 2 years and over

  • apply to hands
  • allow to dry without wiping
  • Children under 2 years ask a doctor before use

Other Information

STORAGE AND HANDLING SECTION

Other information

  • store at room temperature
  • may discolor certain fabrics

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients

water, propylene gylcol, gylcerin, PEG-40 hydrogenated castor oil, disodium EDTA, aloe barbadnsis leaf juice, methylparaben, propylparaben

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

32 wipes NDC 77125-003-01 wet wipes labelwet wipes label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043348benzethonium Cl 0.3 % Medicated PadPSN1
1043348benzethonium chloride 3 MG/ML Medicated PadSCD1
1043348benzethonium chloride 0.3 % Medicated WipeSY1
1043348benzethonium chloride 0.3 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77125-003-012021-07-23C16284748780-1c7ccaba7-140a-fd44-e053-dadaa90aa01bWet Wipes Antibacterial Hand Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77125-003-01Wet Wipes Antibacterial Hand Wipes150 g in 1 BAGSWAB1501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77125-003WET WIPES ANTIBACTERIAL HAND WIPES (BENZETHONIUM CHLORIDE) SWAB [NINGBO YINZHOU GREENLIGHT INTERNATIONAL TRADE CO.,LTD]1Legacy NDC, 1 package rows20200507_a50009ae-7b49-0900-e053-2995a90af023.zip

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
77125-00377125-003-01

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
EDETATE DISODIUM7FLD91C86KIACT
ALOE VERA LEAFZY81Z83H0XIACT
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT
WATER059QF0KO0RIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
GLYCERINPDC6A3C0OXIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB

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
a50009ae-7b4a-0900-e053-2995a90af023a50009ae-7b49-0900-e053-2995a90af0232020-05-06WarningsExact identifier
spl id: a50009ae-7b4a-0900-e053-2995a90af023
spl set id: a50009ae-7b49-0900-e053-2995a90af023

Reported adverse events (FAERS/openFDA)#

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