Ultra-Care Alcohol Prep pad

Manufacturer: Arise Medical LLC
Effective date: 2020-01-28
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:03:30

Label at a glance#

ProductUltra-Care Alcohol Prep pad

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 Ingredient

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

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

in the eyes or on mucous membrane

Consult a Doctor

OTC - ASK DOCTOR SECTION

In case of deep or punctured wounds

Caution

PRECAUTIONS SECTION

Do not apply to irritated skin

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

wipe injection site vigorously

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Water

Other Information

STORAGE AND HANDLING SECTION

Store at room temperature

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 72217-001-01

Ultra-Care Alcohol Prep Pads

MEDIUM 2-PLY PREP PAD

STERILIZED WITH GAMMA RADIATION

Latex FREE

100

Label 1

NDC: 72217-001-02

Ultra-Care Alcohol Prep Pads

MEDIUM 2-PLY PREP PAD

STERILIZED WITH GAMMA RADIATION

Latex FREE

200

Label 2

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
797544	isopropyl alcohol 70 % Medicated Pad	PSN	2
797544	isopropyl alcohol 0.7 ML/ML Medicated Pad	SCD	2
797544	isopropyl alcohol 70 % Medicated Pad	SY	2
797544	isopropyl alcohol 70 % Topical Cloth	SY	2
797544	isopropyl alcohol 70 % Topical Swab	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72217-001-01	2022-01-28	C162847	48780-1	d6a99b39-3846-a426-e053-dadaa90af4c2	68c26c14-772e-42d4-9066-330b1c930c02
72217-001-02	2022-01-28	C162847	48780-1	d6a99b39-3846-a426-e053-dadaa90af4c2	68c26c14-772e-42d4-9066-330b1c930c02

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
72217-001-01	Ultra-Care Alcohol Prep pad	100 in 1 BOX	SWAB	100	2
72217-001-01	Ultra-Care Alcohol Prep pad	70 mL in 1 PACKET	SWAB	70	2
72217-001-02	Ultra-Care Alcohol Prep pad	200 in 1 BOX	SWAB	200	2
72217-001-02	Ultra-Care Alcohol Prep pad	70 mL in 1 PACKET	SWAB	70	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72217-001	ULTRA-CARE ALCOHOL PREP PAD (ISOPRPOPYL ALCOHOL) SWAB [ARISE MEDICAL LLC]	2	Legacy NDC, 4 package rows	20200129_68c26c14-772e-42d4-9066-330b1c930c02.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
72217-001-01	EA - Each	72217-001	42a75268-590a-4e83-8559-710ebd6476f5	1	2024-05-16

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Ultra-Care Alcohol Prep pad
Isoprpopyl Alcohol
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72217-001	72217-001-01, 72217-001-02

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
Name	UNII	Kind
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
WATER	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d8a9fc15-6a7b-4a8c-9864-1fe139bf91df			68c26c14-772e-42d4-9066-330b1c930c02	2020-01-28	Warnings	Exact identifier spl id: d8a9fc15-6a7b-4a8c-9864-1fe139bf91df spl set id: 68c26c14-772e-42d4-9066-330b1c930c02

Reported adverse events (FAERS/openFDA)#

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