FDA.reportPublic FDA data

Hand Antibacterial Wipes

Manufacturer
Ningbo Riway Industrial Co., Ltd.
Effective date
2023-11-21
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 21:20:18

Label at a glance#

ProductHand Antibacterial Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure16 sections

Dosage and administration

Tear open packet, remove wipe. Wet hands thoroughly with product and let hands air dry. Throw used wipe in trash. Do not flush.

Storage and handling

Adults and children 2 years and over. Apply to hands. Allow skin to dry without Wiping. Children under 2 years. Ask a doctor before use.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antimicrobial Agent

Use

INDICATIONS & USAGE SECTION

Decreases 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.

OTC - WHEN USING SECTION

Using this product do not get into eyes. lf contact occurs, rinse thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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

Tear open packet, remove wipe.

Wet hands thoroughly with product and let hands air dry.

Throw used wipe in trash.

Do not flush.

Other information

STORAGE AND HANDLING SECTION

Adults and children 2 years and over.

Apply to hands.

Allow skin to dry without Wiping.

Children under 2 years. Ask a doctor before use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

C12-14 Alkyl Dimethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene Glycol, Aqua.

Hand Antibacterial Wipes Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

40 g in 1 Bag(10 Wipes),NDC:77267-003-05

label 10label 10

353 g in 1 Bag(80 Wipes),NDC:77267-003-06 label 80label 80

538 g in 1 Pail(160 Wipes),NDC:77267-003-03

label 160label 160

1368 g in 1 Pail(500 Wipes),NDC:77267-003-04

label 500label 500

36 g in 1 Bag(10 Wipes),NDC:77267-003-07

label-10-JW-2label-10-JW-2

36 g in 1 Bag(10 Wipes),NDC:77267-003-08 label-10-PB-2label-10-PB-2

2700 g in 1 Bag(1000 Wipes),NDC:77267-003-09

1000pcs Hand Antibacterial Wipes1000pcs Hand Antibacterial Wipes

538 g in 1 Pail(160 Wipes),NDC:77267-003-10

Purigen Hand Sanitizing Wipes 160 wipesPurigen Hand Sanitizing Wipes 160 wipes

1368 g in 1 Pail(500 Wipes),NDC:77267-003-11 Purigen Hand Sanitizing Wipes 500 wipesPurigen Hand Sanitizing Wipes 500 wipes

1800 g in 1 Pail(500 Wipes),NDC:77267-003-12

label-500 15x20cmlabel-500 15x20cm

Hand sanitizing wipes package label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

96g in 1 Bag(25 wipes), NDC:77267-003-13

Inner bag 25pcsInner bag 25pcs165x115x140 for 6 pouch165x115x140 for 6 pouch165x185x140 for 10 pouch165x185x140 for 10 pouch165x290x140mm for 16 pouch165x290x140mm for 16 pouch

4g in 1 Pouch(1 wipe), NDC:77267-003-14

120 inner pouch 1120 inner pouch 123x8.2x12.3cm outer packing box 120pcs23x8.2x12.3cm outer packing box 120pcs

Allure All-Purpose Wipes Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC:77267-003-15

Allure All-Purpose WipesAllure All-Purpose Wipes

Multi-purpose Disinfecting Wipes

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Disinfecting Wipes Tub Die Cut newDisinfecting Wipes Tub Die Cut new

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77267-003HAND ANTIBACTERIAL WIPES (BENZALKONIUM CHLORIDE) CLOTH [NINGBO RIWAY INDUSTRIAL CO., LTD.]10Legacy NDC20231122_a53f0651-9753-605d-e053-2995a90a48b1.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77267-00377267-003-01, 77267-003-02, 77267-003-03, 77267-003-04, 77267-003-05, 77267-003-06, 77267-003-07, 77267-003-08, 77267-003-09, 77267-003-10, 77267-003-11, 77267-003-12, 77267-003-13, 77267-003-14, 77267-003-15, 77267-003-16

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14)G258TFN61XIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
PROPYLENE GLYCOL6DC9Q167V3IACT
EDETATE DISODIUM7FLD91C86KIACT

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
47250f05-2014-1d27-e063-6394a90a112aa53f0651-9753-605d-e053-2995a90a48b12025-12-29WarningsExact identifier
spl set id: a53f0651-9753-605d-e053-2995a90a48b1

Reported adverse events (FAERS/openFDA)#

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