FDA.reportPublic FDA data

Progress Alcohol Wipes

Manufacturer
Truechoicepack, Corp
Effective date
2020-10-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:33:57

Label at a glance#

ProductProgress Alcohol Wipes
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

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

Dosage and administration

Open lid, gently pull back resealable label, remove and use wipe as required. Reseal back after use to avoid evaporation of alcohol.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% by volume

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on 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.

When using this product

OTC - WHEN USING SECTION

do not use in or contact the eyes.

Stop use and ask a doctor if

OTC - STOP USE SECTION

too much skin irritation or sensitivity develops or increases.

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 immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Open lid, gently pull back resealable label, remove and use wipe as required.
  • Reseal back after use to avoid evaporation of alcohol.

Other information

SPL UNCLASSIFIED SECTION

  • Store at room temperature 15°-30°C (59°-86°F).
  • Lot No. Manufacture date and Expiration date can be found on package.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BottleBottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80882-001-502022-01-28C16284748780-1d6a99b39-e507-a426-e053-dadaa90af4c2Progress Alcohol Wipes

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80882-001-50Progress Alcohol Wipes4.04 mL in 1 PATCHCLOTH4.041
80882-001-50Progress Alcohol Wipes50 in 1 BAGCLOTH501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80882-001PROGRESS ALCOHOL WIPES (ALCOHOL) CLOTH [TRUECHOICEPACK, CORP]1Legacy NDC, 2 package rows20201120_b295d74b-1f95-07d2-e053-2a95a90a68eb.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
80882-00180882-001-50

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
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
b295dbac-db41-5b52-e053-2995a90a5813b295d74b-1f95-07d2-e053-2a95a90a68eb2020-10-26WarningsExact identifier
spl id: b295dbac-db41-5b52-e053-2995a90a5813
spl set id: b295d74b-1f95-07d2-e053-2a95a90a68eb

Reported adverse events (FAERS/openFDA)#

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