ISOPROPYL ALCOHOL

Manufacturer: Degasa, S.A. de C.V.
Effective date: 2023-11-05
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:58:58

Label at a glance#

ProductISOPROPYL ALCOHOL

Active ingredientISOPROPYL ALCOHOL

Label structure8 sections

Indications and uses

First aid to help prevent the risk of infection in: Minor cuts Scrapes Burns

Dosage and administration

Clean the affected area. Apply a small amount of product on the area 1 o 3 times daily May be covered with a sterile bandage. If bandaged, let dry first.

Contacts and useful links#

PhoneLabel contact956 728-8899

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 91%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in:

Minor cuts
Scrapes
Burns

Warnings

WARNINGS SECTION

For external use onlyFlammable

Keep away from fire or flame, heat, spark, electrical

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep or puncture wounds, animal bites or serious burns

When using this product

OTC - WHEN USING SECTION

Do not get into eyes
Do not inhale
Do not apply over large areas of the body
Do not use longer than 1 week

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition persists or gets 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 right away.

Caution

PRECAUTIONS SECTION

Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected area.
Apply a small amount of product on the area 1 o 3 times daily
May be covered with a sterile bandage.
If bandaged, let dry first.

Other Information

SPL UNCLASSIFIED SECTION

Does not contain, nor is intended as a substitute for grain or ethyl alcohol
Will produce serious gastric disturbances if taken internally

Question or comments?

OTC - QUESTIONS SECTION

Call 956 728-8899

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bottle

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582901	isopropyl alcohol 91 % Topical Solution	PSN	2
582901	isopropyl alcohol 0.91 ML/ML Topical Solution	SCD	2
582901	isopropyl alcohol 91 % Topical Solution	SY	2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67326-035-00	ISOPROPYL ALCOHOL	473 mL in 1 BOTTLE	LIQUID	473		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67326-035	ISOPROPYL ALCOHOL LIQUID [DEGASA, S.A. DE C.V.]	2	Current NDC, Legacy NDC, 1 package rows	20231106_5fd376ec-d58a-41e3-b974-38527d15c7a8.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
67326-035	67326-035-00

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	Degasa, S.A. de C.V.	5fd376ec-d58a-41e3-b974-38527d15c7a8	2023-11-05	Warnings	Exact identifier ndc (package): 67326-035-00 ndc (product): 67326-035 ndc11 (package): 67326003500 spl id: 09732ce9-588a-26f2-e063-6394a90a9144 spl set id: 5fd376ec-d58a-41e3-b974-38527d15c7a8

Reported adverse events (FAERS/openFDA)#

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