Alcohol Prep Pads

Manufacturer
Phoenix Healthcare Solutions LLC | Phoenix Innovative Healthcare Manufacturers Private Limited
Effective date
2025-10-23
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:40:35

Label at a glance#

ProductAlcohol Prep Pads
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Storage and handling

Store at 4-35C. Avoid direct sunlight.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% by volume

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

For preparation of the skin prior to injection

WARNINGS SECTION

For external use only. Flammable, keep away from fire or flame.

OTC - DO NOT USE SECTION

Do not use with electocautery procedures, or in/near eyes.

OTC - STOP USE SECTION

Stop use if irritation or redness develops. If irritating condition persists for more than 72 hours, consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical attention and/or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Prepare site by wiping vigorously.

STORAGE AND HANDLING SECTION

Store at 4-35C. Avoid direct sunlight.

INACTIVE INGREDIENT SECTION

Purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBox

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN6
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD6
797544isopropyl alcohol 70 % Medicated PadSY6
797544isopropyl alcohol 70 % Topical ClothSY6
797544isopropyl alcohol 70 % Topical SwabSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60913-206-02Alcohol Prep Pads100 in 1 CARTONSWAB1006
60913-206-02Alcohol Prep Pads1 mL in 1 PACKETSWAB16

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
60913-20660913-206-02

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
52024-10-17full-release2026-06-01 00:27:15

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 LLCc92524fd-8b91-592d-e053-2a95a90a88c62025-10-23WarningsExact identifier
ndc (package): 60913-206-02
ndc (product): 60913-206
ndc11 (package): 60913020602
spl id: 41d13f3b-e117-1ca2-e063-6394a90a2718
spl set id: c92524fd-8b91-592d-e053-2a95a90a88c6

Reported adverse events (FAERS/openFDA)#

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