Alcohol Prep Pads

Manufacturer: PHOENIX HEALTHCARE SOLUTIONS, LLC
Effective date: 2025-10-23
Label type: HUMAN OTC DRUG LABEL
Version: 17
Source: full-release
Hydrated at: 2026-06-01 01:29:22

Label at a glance#

ProductAlcohol Prep Pads

Active ingredientISOPROPYL ALCOHOL

Label structure8 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 skin prior to injection; to decrease germs in minor cuts and scrapes.

Warnings:

WARNINGS SECTION

For external use only. Flammable; keep away from fire and flame.

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.

Caution:

OTHER SAFETY INFORMATION

Do not apply to irritated skin.

Do not use

OTC - DO NOT USE SECTION

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 ingredients:

INACTIVE INGREDIENT SECTION

Water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 60913-006-01

Phoenix Healthcare Solutions,LLC

An Innovative Medical Manufacturer

100 Individual Pads

Alcohol Prep Pads

Sterile Medium

For Individual, Professional and Hospital Use

Saturated with 70% v/v Isopropyl Alcohol for external use only

Latex Free

Sterile in unopened, undamaged package

Spunlace non-woven

Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
797544	isopropyl alcohol 70 % Medicated Pad	PSN	17
797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD	17
797544	isopropyl alcohol 70 % Medicated Pad	SY	17
797544	isopropyl alcohol 70 % Topical Cloth	SY	17
797544	isopropyl alcohol 70 % Topical Swab	SY	17

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
60913-006-01	Alcohol Prep Pads	1 mL in 1 PACKET	SWAB	1		17
60913-006-01	Alcohol Prep Pads	100 in 1 CARTON	SWAB	100		17

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
60913-006-01	EA - Each	60913-006	6cd459e5-0dac-437c-a00e-5f057e6f9245	1	2014-02-04

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ISOPROPYL ALCOHOL	ACTIVE INGREDIENT	ND2M416302	8
ISOPROPYL ALCOHOL	ACTIVE MOIETY	ND2M416302	8
WATER	INACTIVE INGREDIENT	059QF0KO0R	8

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Alcohol Prep Pads
Isopropyl Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
60913-006	60913-006-01

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	ACTIB

Source Document#

Source XML · Source PDF

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
LEUPROLIDE ACETATE	LEUPROLIDE ACETATE	Eugia US LLC	49a1d0c1-304c-46f2-a780-bd940ae1ced0	2026-05-08	Warnings, Adverse reactions	Exact identifier ndc (package): 60913-006-01 ndc11 (package): 60913000601
Alcohol Prep Pads	ISOPROPYL ALCOHOL	PHOENIX HEALTHCARE SOLUTIONS, LLC	a225426a-c4d5-459c-bc11-2b521e08e510	2025-10-23	Warnings	Exact identifier ndc (package): 60913-006-01 ndc (product): 60913-006 ndc11 (package): 60913000601 spl id: 41d33f73-9af5-41b7-e063-6394a90aacd0 spl set id: a225426a-c4d5-459c-bc11-2b521e08e510

Reported adverse events (FAERS/openFDA)#

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