FDA.reportPublic FDA data

Alcohol Prep pad

Manufacturer
NDC National Distribution & Contracting, Inc. | Dukal
Effective date
2023-03-15
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:54:29

Label at a glance#

ProductAlcohol Prep pad
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Dosage and administration

Wipe injection site vigorously and discard.

Storage and handling

Other Information Store at Room Temperature 15 - 30 C (59 - 86 F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic Cleanser

Use

INDICATIONS & USAGE SECTION

For Preparation of Skin prior to an injection

WARNINGS SECTION

Warnings

  • For External Use Only
  • Flammable, Keep away from fire or flame

OTC - DO NOT USE SECTION

Do Not Use

  • with electrocautery procedures
  • In the Eyes. If contact occurs, flush eyes with water

OTC - STOP USE SECTION

Stop Use

If irritation and redness develop. If condition persists, consult your health care practitioner.

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 injection site vigorously and discard.

STORAGE AND HANDLING SECTION

Other Information

Store at Room Temperature 15 - 30 C (59 - 86 F)

INACTIVE INGREDIENT SECTION

Inactive Ingredient

purified water

PRINCIPAL DISPLAY PANEL - 100 Pouch Box Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REF: P902050

Sterile

Alcohol
Prep Pads

Large (1.75 IN × 3.5 IN)

For Professional and Hospital Use

Sterile unless package is opened or damaged.
Do not resterilize.

Pro
Advantage ®
by NDC

10 boxes/case | 100/box

PRINCIPAL DISPLAY PANEL - 100 Pouch Box LabelPRINCIPAL DISPLAY PANEL - 100 Pouch Box Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN5
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD5
797544isopropyl alcohol 70 % Medicated PadSY5
797544isopropyl alcohol 70 % Topical ClothSY5
797544isopropyl alcohol 70 % Topical SwabSY5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
43128-050-012025-01-30C16284748780-12cef2736-72eb-d83d-e063-dadaa90ab31fSterile Alcohol Prep Pads
43128-050-022025-01-30C16284748780-12cef2736-72eb-d83d-e063-dadaa90ab31fSterile Alcohol Prep Pads

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43128-050-01Alcohol Prep pad1 mL in 1 POUCHSWAB15
43128-050-01Alcohol Prep pad100 in 1 BOXSWAB1005
43128-050-02Alcohol Prep pad200 in 1 BOXSWAB2005
43128-050-02Alcohol Prep pad1 mL in 1 POUCHSWAB15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
43128-050ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) SWAB [NDC NATIONAL DISTRIBUTION & CONTRACTING, INC.]5Legacy NDC, 4 package rows20230316_8cb6d305-289a-4f76-8ee7-adaf9a5ab61e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Isopropyl AlcoholACTIVE INGREDIENTND2M4163021
Isopropyl AlcoholACTIVE MOIETYND2M4163021
waterINACTIVE INGREDIENT059QF0KO0R1

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
43128-05043128-050-01, 43128-050-02

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
f6f20cca-1cc5-7668-e053-6394a90a58b98cb6d305-289a-4f76-8ee7-adaf9a5ab61e2023-03-15WarningsExact identifier
spl id: f6f20cca-1cc5-7668-e053-6394a90a58b9
spl set id: 8cb6d305-289a-4f76-8ee7-adaf9a5ab61e

Reported adverse events (FAERS/openFDA)#

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