Aerowipe

Manufacturer: Aero Healthcare
Effective date: 2025-07-10
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:07:01

Label at a glance#

ProductAerowipe

Active ingredientISOPROPYL ALCOHOL

Label structure10 sections

Dosage and administration

Apply topically to cleanse the intended area and discard after single use.

Label contents#

Full prescribing information#

Use:

INDICATIONS & USAGE SECTION

To help prevent infection in minor cuts and scrapes

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol, 70% v/v

Warnings:

WARNINGS SECTION

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

Do not use:

OTC - DO NOT USE SECTION

Longer than 1 week
In the eyes

Stop Use:

OTC - STOP USE SECTION

If irritation and redness develop. If condition persists consult your 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.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply topically to cleanse the intended area and discard after single use.

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Purified Water

Purpose

OTC - PURPOSE SECTION

Antiseptic

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AW7001 Label

AEROWIPE Alcohol Swab

LOT XXXXX

EXP XXXXXX

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 Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55305-120-01	2025-07-10	C162847	48780-1	9d75b9d0-9a15-f424-e053-dadaa90a57ce	AEROWIPE - Alcohol Swab
55305-120-02	2025-07-10	C162847	48780-1	9d75b9d0-9a15-f424-e053-dadaa90a57ce	AEROWIPE - Alcohol Swab
55305-120-01	2020-01-31	C162847	48780-1	9d75b9d0-9a15-f424-e053-dadaa90a57ce	AEROWIPE - Alcohol Swab
55305-120-02	2020-01-31	C162847	48780-1	9d75b9d0-9a15-f424-e053-dadaa90a57ce	AEROWIPE - Alcohol Swab

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
55305-120-01	Aerowipe	0.4 mL in 1 POUCH	SWAB	0.4	2
55305-120-02	Aerowipe	50 in 1 BOX	SWAB	50	2
55305-120-02	Aerowipe	0.4 mL in 1 POUCH	SWAB	0.4	2
55305-120-03	Aerowipe	10 in 1 BAG	SWAB	10	2

Products#

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

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

Aerowipe
Alcohol Wipe
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
55305-120	55305-120-01, 55305-120-03, 55305-120-02

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
Aerowipe	ALCOHOL WIPE	Aero Healthcare	34c93704-9f3c-6746-e054-00144ff8d46c	2025-07-10	Warnings	Exact identifier ndc (package): 55305-120-02 ndc (package): 55305-120-03 ndc (package): 55305-120-01 ndc (product): 55305-120 ndc11 (package): 55305012002 ndc11 (package): 55305012003 ndc11 (package): 55305012001 spl id: 39967f57-908d-ff44-e063-6394a90aceb2 spl set id: 34c93704-9f3c-6746-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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