1166 Isopropyl Alcohol Spray

Manufacturer: Dynarex Corporation
Effective date: 2024-02-15
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:09:02

Label at a glance#

ProductIsopropyl Alcohol

Active ingredientISOPROPYL ALCOHOL

Label structure9 sections

Dosage and administration

• Clean the affected area and spray 1 to 3 times daily • May be covered with a sterile bandage • If bandaged, let dry first • Children under 12 years of age: C onsult a doctor before use

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For External Use Only

Do not use

OTC - DO NOT USE SECTION

• Near eyes or mucous membranes • Over large areas of the body • Longer than 1 week unless directed by a doctor • With electrocautery procedures

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

Deep or puncture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

OTC - STOP USE SECTION

Condition persists for more than 72 hours or get worse.

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Clean the affected area and spray 1 to 3 times daily • May be covered with a sterile bandage • If bandaged, let dry first

• Children under 12 years of age: Consult a doctor before use

Other Information

OTHER SAFETY INFORMATION

• Store at 20º-25ºC

• Avoid excessive heat

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Purified Water

Questions?

OTC - QUESTIONS SECTION

1-888-Dynarex Monday - Friday, 9AM - 5PM EST

Label 1166

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1166_IN_MASTERIsopropyl Alcohol Spray

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1014638	isopropyl alcohol 70 % Topical Spray	PSN	1
1014638	isopropyl alcohol 0.7 ML/ML Topical Spray	SCD	1
1014638	isopropyl alcohol 70 % Topical Spray	SY	1

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67777-011-01	Isopropyl Alcohol	24 in 1 CASE	SPRAY	24		1
67777-011-02	Isopropyl Alcohol	59.1 mL in 1 BOTTLE, SPRAY	SPRAY	59.1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67777-011	ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL SPRAY) SPRAY [DYNAREX CORPORATION]	1	Current NDC, 2 package rows	20240229_116e0c9c-cbe0-bf67-e063-6394a90ae530.zip

Products#

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

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

Isopropyl Alcohol
Isopropyl Alcohol Spray
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
67777-011	67777-011-02, 67777-011-01

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

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 SPRAY	Dynarex Corporation	116e0c9c-cbe0-bf67-e063-6394a90ae530	2024-02-15	Warnings	Exact identifier ndc (package): 67777-011-02 ndc (package): 67777-011-01 ndc (product): 67777-011 ndc11 (package): 67777001101 ndc11 (package): 67777001102 spl id: 116e0c9c-cbe1-bf67-e063-6394a90ae530 spl set id: 116e0c9c-cbe0-bf67-e063-6394a90ae530

Reported adverse events (FAERS/openFDA)#

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