FDA.reportPublic FDA data

Alcohol Wipes

Manufacturer
Ningbo Riway Industrial Co., Ltd.
Effective date
2023-11-21
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
legacy-cache
Hydrated at
2026-08-01 21:20:17

Label at a glance#

ProductAlcohol Wipes
Active ingredientALCOHOL
Label structure13 sections

Dosage and administration

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

Storage and handling

Store between 15-30 °C (59-86 °F). Avoid freezing and excessive heat above 40 °C (104 °F).

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on skin.

Warnings

WARNINGS SECTION

For external use only. Flammable: Keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

In children less than 2 months of age.

On open skin wounds.

OTC - WHEN USING SECTION

When using this product avoid contact with eyes and mouth. If in eyes，flush thoroughly with water.

OTC - STOP USE SECTION

Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Tear open packet and 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

Store between 15-30 °C (59-86 °F).

Avoid freezing and excessive heat above 40 °C (104 °F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water.

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC:77267-002-05 label 10label 10

NDC:77267-002-06 label 80label 80

NDC:77267-002-03 label 160label 160

NDC:77267-002-04 label 500label 500

NDC:77267-002-07

label-200 wipeslabel-200 wipes

NDC:77267-002-08

label-50 packagelabel-50 package

NDC:77267-002-09

label-50 paillabel-50 pailNDC:77267-002-10

label-100 paillabel-100 pailNDC:77267-002-11

label-150 paillabel-150 pail

NDC:77267-002-12

Allure Alcohol WipesAllure Alcohol Wipes

NDC:77267-002-13

1000pcs Advance1000pcs Advance

NDC:77267-002-14

15x20 100pcs pail15x20 100pcs pailNDC:77267-002-15

18x20 50pcs pouch18x20 50pcs pouch18x20 50pcs-4 box18x20 50pcs-4 box

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77267-002ALCOHOL WIPES (ALCOHOL) CLOTH [NINGBO RIWAY INDUSTRIAL CO., LTD.]7Legacy NDC20231122_a53eaa99-3c3d-01a9-e053-2a95a90a7ca4.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77267-00277267-002-01, 77267-002-02, 77267-002-03, 77267-002-04, 77267-002-05, 77267-002-06, 77267-002-07, 77267-002-08, 77267-002-09, 77267-002-10, 77267-002-11, 77267-002-12, 77267-002-13, 77267-002-14, 77267-002-15

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB

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
47117404-7aca-649f-e063-6294a90a70bba53eaa99-3c3d-01a9-e053-2a95a90a7ca42025-12-29WarningsExact identifier
spl set id: a53eaa99-3c3d-01a9-e053-2a95a90a7ca4

Reported adverse events (FAERS/openFDA)#

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