Isopropyl Rubbing Alcohol

Manufacturer: NDC, Inc.
Effective date: 2026-01-08
Label type: HUMAN OTC DRUG LABEL
Version: 12
Source: monthly-update
Hydrated at: 2026-06-03 17:52:37

Label at a glance#

ProductIsopropyl Rubbing Alcohol

Active ingredientISOPROPYL ALCOHOL

Label structure9 sections

Indications and uses

First aid to help prevent the risk of infection in: minor cuts scrapes burns

Dosage and administration

clean infected area apply 1 to 3 times daily

Contacts and useful links#

Websitewww.proadvantagebyndc.com

www.ProAdvantagebyNDC.com

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in:

minor cuts
scrapes
burns

WARNINGS

WARNINGS SECTION

For external use only

Flammable

SPL UNCLASSIFIED SECTION

keep away from fire or flame, heat, spark, electrical. Flash point 72°F
do not use with electrocautery procedures.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you havedeep or puncture wounds, animal bites or serious burns.

When using this product

OTC - WHEN USING SECTION

do not get into eyes
do not apply over large areas of the body
do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

the condition persists or gets worse

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

clean infected area
apply 1 to 3 times daily

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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Purified Water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REF: P907132

NDC 43128-002-32

Pro
ADVANTAGE®

Isopropyl Rubbing
Alcohol 70% USP

Tamper evident cap for your protection.
If ring-band is detached from cap or missing do not use.

WARNING:Flammable

Made in USA for:
NDC, Inc., 407 New Sanford Rd.
La Vergne, TN 37086
www.ProAdvantagebyNDC.com

32 fl. oz. (946 mL)

PRINCIPAL DISPLAY PANEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
808520	isopropyl alcohol 70 % Topical Solution	PSN	12
808520	isopropyl alcohol 0.7 ML/ML Topical Solution	SCD	12
808520	isopropyl alcohol 70 % Topical Solution	SY	12

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	SPL version
43128-002-01	Isopropyl Rubbing Alcohol	3785 mL in 1 BOTTLE, PLASTIC	SOLUTION	3785	12
43128-002-16	Isopropyl Rubbing Alcohol	473 mL in 1 BOTTLE, PLASTIC	SOLUTION	473	12
43128-002-32	Isopropyl Rubbing Alcohol	946 mL in 1 BOTTLE, PLASTIC	SOLUTION	946	12

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Isopropyl Alcohol	ACTIVE INGREDIENT	ND2M416302	1
Isopropyl Alcohol	ACTIVE MOIETY	ND2M416302	1
Water	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

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

Isopropyl Rubbing Alcohol
Isopropyl Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
43128-002	43128-002-32, 43128-002-01, 43128-002-16

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

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
11	2024-11-15	full-release	2026-06-01 00:37:17

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 Rubbing Alcohol	ISOPROPYL ALCOHOL	NDC, Inc.	07bfadf4-7452-4c7a-b60e-feb658b92e73	2026-01-08	Warnings	Exact identifier ndc (package): 43128-002-16 ndc (package): 43128-002-32 ndc (package): 43128-002-01 ndc (product): 43128-002 ndc11 (package): 43128000201 ndc11 (package): 43128000232 ndc11 (package): 43128000216 spl id: 47e5c09a-4f6a-9963-e063-6394a90a3476 spl set id: 07bfadf4-7452-4c7a-b60e-feb658b92e73

Reported adverse events (FAERS/openFDA)#

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