69103-5500, Isopropyl alcohol spray

Manufacturer: Provision Medical | : Safetec of America, Inc. | Safetec of America, Inc.
Effective date: 2024-03-14
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 00:10:10

Label at a glance#

ProductIsopropyl Alcohol

Active ingredientISOPROPYL ALCOHOL

Label structure7 sections

Indications and uses

First aid to help prevent infection in minor cuts, scrapes and burns

Dosage and administration

spray over cleaned affected area 1 to 3 times daily

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent infection in minor cuts, scrapes and burns

Warnings

WARNINGS SECTION

For external use only.

Flammable keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

near eyes or mucous membranes
on deep or puncture wounds, animal bites or serious burns

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Caution

not for use on large areas of the body
if redness, irritation, swelling or pain persists or increases, discontinue use and consult a physician.

Directions

DOSAGE & ADMINISTRATION SECTION

spray over cleaned affected area 1 to 3 times daily

Inactive Ingredients

INACTIVE INGREDIENT SECTION

purified water

Principal Display Panel – 2 fl. oz Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The Provision
First Aid
Line™

Isopropyl
Alcohol Spray

First Aid to Help
Prevent Infection in
Minor Cuts, Scrapes
and Burns.

2 fl. oz. (59.1 ml)

Reorder no. 3502

Principal Display Panel – 2 fl. oz Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1014638	isopropyl alcohol 70 % Topical Spray	PSN	2
1014638	isopropyl alcohol 0.7 ML/ML Topical Spray	SCD	2
1014638	isopropyl alcohol 70 % Topical Spray	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
69103-5500-0	2024-03-20	C162847	48780-1	1030e365-1e79-111a-e063-dadaa90a10e2	69103-5500, Isopropyl alcohol spray
69103-5500-0	2024-01-30	C162847	48780-1	1030e365-1e79-111a-e063-dadaa90a10e2	69103-5500, Isopropyl alcohol spray

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69103-5500-0	Isopropyl Alcohol	0.0591 L in 1 BOTTLE, SPRAY	SPRAY	0.0591		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69103-5500	ISOPROPYL ALCOHOL SPRAY [PROVISION MEDICAL]	2	Current NDC, Legacy NDC, 1 package rows	20240322_ad045374-f4ad-4003-b350-8a2b0cbccb2e.zip

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

Isopropyl Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69103-5500	69103-5500-0

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

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
Isopropyl Alcohol	ISOPROPYL ALCOHOL	Provision Medical	ad045374-f4ad-4003-b350-8a2b0cbccb2e	2024-03-14	Warnings	Exact identifier ndc (package): 69103-5500-0 ndc (product): 69103-5500 ndc11 (package): 69103550000 spl id: 13a3cf2a-ee3b-be81-e063-6294a90a2981 spl set id: ad045374-f4ad-4003-b350-8a2b0cbccb2e

Reported adverse events (FAERS/openFDA)#

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