FDA.reportPublic FDA data

Wipes Plus

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 23:51:11

Label at a glance#

ProductWipes Plus
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

• For hand sanitizing to decrease bacteria on the skin. • Apply topically to the skin to help prevent cross contamination. • Recommended for repeated use. • Dries In seconds.

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% by volume

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.
• Recommended for repeated use.
• Dries In seconds.

Warnings

WARNINGS SECTION

  • Flammable, keep away from fire or flame. For external use only.
  • Do not use In or contact the eyes.
  • Discontinue use If redness or Irritation develops.
  • If condition persists for more than 72 hours, consult a physician.

Keep our of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of chlldren unless under adult supervision.

Directions

DOSAGE & ADMINISTRATION SECTION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Propylene Glycol, Glycerin, Carboner, Aminomethyl Propanol, Aloe Barbadenis Leaf Juice, Tocopheryl Acetate.

Questions or Comments

OTC - QUESTIONS SECTION

Lot No. and Expiration Date can be found on canister.

@PROGRESSIVE PRODUCTS, LLC
4 International Drive, Rye Brook, NY 1 0573
CGll 914-417-6022
Re-order/Item No. 33884
www.wlpesplus.com

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 67151-606-01

RE-ORDER/ITEM NO 37604

LabelLabel

NDC 67151-606-02

RE-ORDER/ITEM NO 33884

Label 1Label 1

NDC 67151-606-03

RE-ORDER/ITEM NO 37524

Label 2Label 2

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
67151-606-012024-01-30C16284748780-11030e365-52d2-111a-e063-dadaa90a10e2DRUG FACTS
67151-606-022024-01-30C16284748780-11030e365-52d2-111a-e063-dadaa90a10e2DRUG FACTS
67151-606-032024-01-30C16284748780-11030e365-52d2-111a-e063-dadaa90a10e2DRUG FACTS

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67151-606-01Wipes Plus80 in 1 PACKAGESWAB802
67151-606-01Wipes Plus1 mL in 1 PACKAGESWAB12
67151-606-02Wipes Plus1 mL in 1 PACKAGESWAB12
67151-606-02Wipes Plus240 in 1 PACKAGESWAB2402
67151-606-03Wipes Plus1 mL in 1 PACKAGESWAB12
67151-606-03Wipes Plus1500 in 1 PACKAGESWAB15002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
67151-606WIPES PLUS (ALCOHOL) SWAB [PROGRESSIVE PRODUCTS, LLC]2Legacy NDC, 6 package rows20221027_8f4aad39-ce1a-4d83-96bd-d2563f207727.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
67151-60667151-606-01, 67151-606-02, 67151-606-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
AMINOMETHYLPROPANOLLU49E6626QIACT
ALOE VERA LEAFZY81Z83H0XIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
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
eaff2ae9-2f96-309c-e053-2a95a90a9b9a8f4aad39-ce1a-4d83-96bd-d2563f2077272022-10-14WarningsExact identifier
spl id: eaff2ae9-2f96-309c-e053-2a95a90a9b9a
spl set id: 8f4aad39-ce1a-4d83-96bd-d2563f207727

Reported adverse events (FAERS/openFDA)#

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