FDA.reportPublic FDA data

UNITED CleanPlus Sanitizing Wipe

Manufacturer
Jiebao Daily Chemical (Xiangxi)Co.,Ltd
Effective date
2020-08-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:26:00

Label at a glance#

ProductUNITED CleanPlus Sanitizing Wipe
Active ingredientISOPROPYL ALCOHOL
Label structure6 sections

Dosage and administration

Wipe hands thoroughly. Let skin dry and discard Keep out of reach of children under 6 years of age use only under adult supervision. Not recommended for infants

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

ISOPROPYL ALCOHOL ........... 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

  • Help reduce bacteria on the hands

Warning

WARNINGS SECTION

  • Flammable, keep away from fire or flame. 
  • For external use only.

Do not use On open skin wounds

  • When using this product, Do not use in or near the eyes. In case of contact with eyes flush thoroughly with water. USE wipes only on unbroken, instact skin.

    Do not ingest

  • Stop use and ask a doctor if irritatio or redness develops.

Other information:

  • Do not store above 105℉

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

●If swallowed, get medical help or contact a Poison Contrl Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wipe hands thoroughly. Let skin dry and discard
  • Keep out of reach of children under 6 years of age use only under adult supervision.
  • Not recommended for infants

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label imagelabel image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN1
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD1
797544isopropyl alcohol 70 % Medicated PadSY1
797544isopropyl alcohol 70 % Topical ClothSY1
797544isopropyl alcohol 70 % Topical SwabSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78724-010-012024-07-30C16284748780-11030e365-5b75-111a-e063-dadaa90a10e2Wipes
78724-010-012024-01-30C16284748780-11030e365-5b75-111a-e063-dadaa90a10e2Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78724-010-01UNITED CleanPlus Sanitizing Wipe5 g in 1 POUCHSWAB51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78724-010UNITED CLEANPLUS SANITIZING WIPE (ISOPROPYL ALCOHOL) SWAB [JIEBAO DAILY CHEMICAL (XIANGXI)CO.,LTD]1Legacy NDC, 1 package rows20200828_2a8df50b-c41e-4eb2-af99-645fee5923ee.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
78724-01078724-010-01

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
ISOPROPYL ALCOHOLND2M416302ACTIB
water059QF0KO0RIACT

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
0e9423eb-aa0a-4edc-91f7-32e8a844f7572a8df50b-c41e-4eb2-af99-645fee5923ee2020-08-28WarningsExact identifier
spl id: 0e9423eb-aa0a-4edc-91f7-32e8a844f757
spl set id: 2a8df50b-c41e-4eb2-af99-645fee5923ee

Reported adverse events (FAERS/openFDA)#

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