FDA.reportPublic FDA data

Alcohol Prep Pad

Manufacturer
Total Resource
Effective date
2023-11-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:21:17

Label at a glance#

ProductAlcohol Prep Pad
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Dosage and administration

Wipe Injection site vigorously and discard.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For preparation of skin prior to injection.

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame

Do not use:

OTC - DO NOT USE SECTION

  • with electrocautery procedures
  • in the eyes.
  • on mucous membranes
  • on irritated skin.

Stop use

OTC - STOP USE SECTION

Stop use and ask a doctor If irritation or redness develops.

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

Wipe Injection site vigorously and discard.

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature 59° - 86°F (15° - 30°C)

Inactive ingredient

INACTIVE INGREDIENT SECTION

water

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packaging FrontPackaging FrontDrug Facts ContinuedDrug Facts Continued

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
55550-80155550-801-01

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
25120111-4ad0-7061-e063-6394a90a8f5ca966859f-bf96-5d66-e053-2a95a90a9b582024-10-22WarningsExact identifier
spl set id: a966859f-bf96-5d66-e053-2a95a90a9b58

Reported adverse events (FAERS/openFDA)#

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