FDA.reportPublic FDA data

Adhesive Remover Wipes

Manufacturer
Ningbo Riway Industrial Co., Ltd.
Effective date
2024-03-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:07:10

Label at a glance#

ProductAdhesive Remover Wipes
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Dosage and administration

Tear open packet and remove wipe. Wipe the skin thoroughly. Throw used wipe in trash. Do not flush.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 1%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For the removal of adhesive residue on skin.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

If you are allergic to any of the ingredients.

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Discontinue use and contact a doctor if irritation and redness develop and condition persists 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.

Wipe the skin thoroughly.

Throw used wipe in trash. Do not flush.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Extract,Ethylhexylglycerin,Iodopropynyl Butylcarbamate,Isododecane,Phenoxyethanol,Purified water,Tocopheryl Acetate

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pouch-1pouch-1

box-50box-50

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77267-006ADHESIVE REMOVER WIPES (ISOPROPYL ALCOHOL) CLOTH [NINGBO RIWAY INDUSTRIAL CO., LTD.]3Legacy NDC20240329_b1a9c2ab-6761-ebe1-e053-2995a90aa338.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77267-00677267-006-01, 77267-006-02

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
FRAGRANCE LAVENDER & CHIA F-153480SXS9CO2TZKIACT
ALOE VERA LEAFZY81Z83H0XIACT
IODOPROPYNYL BUTYLCARBAMATE603P14DHEBIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ISOPROPYL ALCOHOLND2M416302ACTIB
ETHYLHEXYLGLYCERIN147D247K3PIACT
ISODODECANEA8289P68Y2IACT
WATER059QF0KO0RIACT
PHENOXYETHANOLHIE492ZZ3TIACT

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
472666bc-1c14-d03d-e063-6394a90a9ed6b1a9c2ab-6761-ebe1-e053-2995a90aa3382025-12-30WarningsExact identifier
spl set id: b1a9c2ab-6761-ebe1-e053-2995a90aa338

Reported adverse events (FAERS/openFDA)#

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