FDA.reportPublic FDA data

Wipesplus Hand Sanitizing Wipes

Manufacturer
Progressive Products, LLC
Effective date
2022-10-14
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:51:02

Label at a glance#

ProductWipesplus Hand Sanitizing Wipes
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin. Apply topically to the skin to help prevent cross contamination Not recommended for repeated use. Dries in seconds.

Dosage and administration

Remove lid. Pull wipe from center of roll and thread theough opening in lid. Do not push finger through opening. Replace lid, pull wipe up, and then at 45° angle. The next wipe dispenses automatically. Close lid to retain moisture.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin.
  • Apply topically to the skin to help prevent cross contamination
  • Not recommended for repeated use.
  • Dries in seconds.

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

SAFE HANDLING WARNING SECTION

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • in or near the eyes
  • on open skin wounds or burns.

Stop use and ask a doctor

OTC - STOP USE SECTION

  • if irritation and redness develop
  • condition persists for more than 72 hours.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Remove lid.
  • Pull wipe from center of roll and thread theough opening in lid. Do not push finger through opening.
  • Replace lid, pull wipe up, and then at 45° angle. The next wipe dispenses automatically.
  • Close lid to retain moisture.

Other Information

OTHER SAFETY INFORMATION

  • Store at room temperature.
  • Dispose of used wipe in trash, do not flush into toilet.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Extract, Benzalkonium Chloride, Citric Acid, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

wipesplus

HAND SANITIZING WIPES

  • Killes 99.9% of germs

240 CT

artwork 1artwork 1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1489307ethanol 70 % Medicated PadPSN2
1489307ethanol 0.7 ML/ML Medicated PadSCD2
1489307ethanol 70 % Medicated PadSY2
1489307ethanol 70 % Medicated WipesSY2
1489307ethyl alcohol 70 % ClothSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
67151-737-012024-01-30C16284748780-11030e365-2575-111a-e063-dadaa90a10e2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67151-737-01Wipesplus Hand Sanitizing Wipes240 in 1 PACKAGECLOTH2402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67151-737WIPESPLUS HAND SANITIZING WIPES (ETHYL ALCOHOL) CLOTH [PROGRESSIVE PRODUCTS, LLC]2Legacy NDC, 1 package rows20221015_e3b4177e-8650-1446-e053-2a95a90a5aac.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
67151-73767151-737-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT

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
eaff3d91-549d-68f8-e053-2995a90aea40e3b4177e-8650-1446-e053-2a95a90a5aac2022-10-14WarningsExact identifier
spl id: eaff3d91-549d-68f8-e053-2995a90aea40
spl set id: e3b4177e-8650-1446-e053-2a95a90a5aac

Reported adverse events (FAERS/openFDA)#

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