FDA.reportPublic FDA data

Alcohol Prep Pads

Manufacturer
Phoenix Healthcare Solutions LLC
Effective date
2025-10-23
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:29:31

Label at a glance#

ProductAlcohol Prep Pads
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Dosage and administration

Wipe injection site Vigorously

Storage and handling

Store at Room Temperature

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For preparation of the Skinprior to injection, to decrease germs in minor cuts & scrap.

Warning

WARNINGS SECTION

For External Use Only. Flammable, Keep away from fire & flame.

Keep out of reach of Children

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 Immediately.

Caution

OTHER SAFETY INFORMATION

Do not apply to irritated Skin

Do not use

OTC - DO NOT USE SECTION

Do not use in the eyes, or on mucous membranes. In case of deep or puncture wounds, consult a doctor.

Directions

DOSAGE & ADMINISTRATION SECTION

Wipe injection site Vigorously

Other Information

STORAGE AND HANDLING SECTION

Store at Room Temperature

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water

Principal display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CT100CT100CT200CT200CT300CT300CT400CT400

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN4
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD4
797544isopropyl alcohol 70 % Medicated PadSY4
797544isopropyl alcohol 70 % Topical ClothSY4
797544isopropyl alcohol 70 % Topical SwabSY4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60913-025-01Alcohol Prep Pads1 mL in 1 PACKETSWAB14
60913-025-01Alcohol Prep Pads100 in 1 CARTONSWAB1004
60913-025-02Alcohol Prep Pads200 in 1 CARTONSWAB2004
60913-025-02Alcohol Prep Pads1 mL in 1 PACKETSWAB14
60913-025-03Alcohol Prep Pads1 mL in 1 PACKETSWAB14
60913-025-03Alcohol Prep Pads300 in 1 CARTONSWAB3004
60913-025-04Alcohol Prep Pads400 in 1 CARTONSWAB4004
60913-025-04Alcohol Prep Pads1 mL in 1 PACKETSWAB14

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
60913-025-01EA - Each60913-02584189a06-917a-4e81-a597-7a874edde55d12024-01-04
60913-025-02EA - Each60913-0254efb6f36-b4a8-4419-b26c-26b50fbc106712024-01-04
60913-025-03EA - Each60913-0256b5d5e33-b82d-48f5-858a-c95354287f1b12024-01-04
60913-025-04EA - Each60913-0256a4f124e-1d82-4b51-a18a-66707c4c441f12024-01-04

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
60913-02560913-025-01, 60913-025-02, 60913-025-03, 60913-025-04

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
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT

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
Alcohol Prep PadsISOPROPYL ALCOHOLPhoenix Healthcare Solutions LLCe917b371-3ca9-94f0-e053-2a95a90af8ad2025-10-23WarningsExact identifier
ndc (package): 60913-025-04
ndc (package): 60913-025-01
ndc (package): 60913-025-03
ndc (package): 60913-025-02
ndc (product): 60913-025
ndc11 (package): 60913002504
ndc11 (package): 60913002501
ndc11 (package): 60913002503
ndc11 (package): 60913002502
spl id: 41d31f44-667a-53bc-e063-6294a90a38cd
spl set id: e917b371-3ca9-94f0-e053-2a95a90af8ad

Reported adverse events (FAERS/openFDA)#

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