Alcohol Prep Pad

Manufacturer: ASO LLC
Effective date: 2024-11-01
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:33:32

Label at a glance#

ProductAlcohol Prep Pad

Active ingredientISOPROPYL ALCOHOL

Label structure11 sections

Indications and uses

For preparation of the skin prior to an injection.

Dosage and administration

wipe ingection area and discard

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For preparation of the skin prior to an 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. If contact occurs, flush eyes with water.

Stop use if

OTC - STOP USE SECTION

irritation and redness develop. If condition continues, consult you health care practitioner.

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 ingection area and discard

Other Information

OTHER SAFETY INFORMATION

Store at room temperature: 59ºF - 86ºF (15ºC - 30ºC)

Inactice ingredient

INACTIVE INGREDIENT SECTION

purified water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

alcohol prep pad

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51142-445-21	Alcohol Prep Pad	0.34 g in 1 POUCH	SWAB	0.34		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51142-445	ALCOHOL PREP PAD SWAB [ASO LLC]	2	Current NDC, 1 package rows	20241103_f2a41151-a807-566c-e053-2995a90af877.zip

Products#

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

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

Alcohol Prep Pad
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51142-445	51142-445-21

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 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Walgreens	DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, LIDOCAINE HCL, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, ETHYL ALCOHOL	Walgreen Co.	5630f48b-404c-b847-e063-6394a90a8d8e	2026-07-09	Warnings	Exact identifier ndc (package): 51142-445-21 ndc11 (package): 51142044521
Care Science	DIPHENHYDRAMINE HYDROCHLORIDE, IBUPROFEN, HYDROCORTISONE, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN-B SULFATE, LIDOCAINE HCL, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, ETHYL ALCOHOL	ASO LLC	562f2b2c-d234-e491-e063-6294a90a705f	2026-07-08	Warnings	Exact identifier ndc (package): 51142-445-21 ndc11 (package): 51142044521
Alcohol Prep Pad	ALCOHOL PREP PAD	ASO LLC	f2a41151-a807-566c-e053-2995a90af877	2024-11-01	Warnings	Exact identifier ndc (package): 51142-445-21 ndc (product): 51142-445 ndc11 (package): 51142044521 spl id: 25da7c3f-0378-96c8-e063-6394a90a52ea spl set id: f2a41151-a807-566c-e053-2995a90af877

Reported adverse events (FAERS/openFDA)#

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