United CleanPlus

Manufacturer
RMT Global Partners, LLC | Yangzhou Suxiang Medical Instrument Co., Ltd
Effective date
2024-10-10
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 20:52:54

Label at a glance#

ProductUnited CleanPlus
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Dosage and administration

Wipe hands thoroughly, let skin dry and discard Keep out of reach of children. Children under 6 years of age use only under adult supervision Not recommended for infants Do not store above 105°F

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 750% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

To reduce bacteria on the skin.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

On open skin wounds

OTC - WHEN USING SECTION

Do not use in or near the eyes. In case of contact with eyes flush thoroughly with water.

Use wipes only on unbroken, intact skin

Do not ingest

OTC - STOP USE SECTION

If skin irritation or redness develops

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

Wipe hands thoroughly, let skin dry and discard

Keep out of reach of children. Children under 6 years of age use only under adult supervision

Not recommended for infants

Do not store above 105°F

Inactive ingredients

INACTIVE INGREDIENT SECTION

pure water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 PSC NDC: 80436-004-011 PSC NDC: 80436-004-01

1 PSC NDC: 80436-004-01

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80436-004UNITED CLEANPLUS (SANITIZING WIPE) CLOTH [RMT GLOBAL PARTNERS, LLC]6Legacy NDC20241012_ae5b1a5e-173b-daa5-e053-2995a90aaff7.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
80436-00480436-004-06, 80436-004-07, 80436-004-08, 80436-004-09, 80436-004-10

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
ISOPROPYL ALCOHOLND2M416302ACTIB

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
4679292e-7284-5001-e063-6294a90a135fae5b1a5e-173b-daa5-e053-2995a90aaff72025-12-21WarningsExact identifier
spl set id: ae5b1a5e-173b-daa5-e053-2995a90aaff7

Reported adverse events (FAERS/openFDA)#

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