Isopropyl Rubbing Alcohol

Manufacturer: Healthwell
Effective date: 2020-10-07
Label type: HUMAN OTC DRUG LABEL
Version: 8
Source: full-release
Hydrated at: 2026-05-31 23:31:10

Label at a glance#

ProductIsopropyl Rubbing Alcohol

Active ingredientISOPROPYL ALCOHOL

Label structure11 sections

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Warnings

WARNINGS SECTION

For external use only

Flammable

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

Do not use with electrocautery procedures

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns

OTC - WHEN USING SECTION

When using this product

do not get into eyes

do ot apply over large areas of the body

do not use longer than 1 week unless directed by a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor if 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 the affected area

Apply a small amount of this product 1 to 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

Inactive Ingredient

INACTIVE INGREDIENT SECTION

purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Isopropyl Rubbing Alcohol 70%

USP FIRST AID ANTISEPTIC

TAMPER EVIDENT CAP FOR YOUR PROTECTION. IF RING-BAND IS DETACHED FROM CAP OR MISSING DO NOT USE.

Manufactured for HealthWell

32 FL OZ

(946 mL)

Isopropyl Alcohol

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
808520	isopropyl alcohol 70 % Topical Solution	PSN	8
808520	isopropyl alcohol 0.7 ML/ML Topical Solution	SCD	8
808520	isopropyl alcohol 70 % Topical Solution	SY	8

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
87010-002-16	2022-01-28	C162847	48780-1	d6a99b39-61d4-a426-e053-dadaa90af4c2	Isopropyl Alcohol
87010-002-32	2022-01-28	C162847	48780-1	d6a99b39-61d4-a426-e053-dadaa90af4c2	Isopropyl Alcohol

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
87010-002-16	Isopropyl Rubbing Alcohol	473 mL in 1 BOTTLE, PLASTIC	SOLUTION	473		8
87010-002-32	Isopropyl Rubbing Alcohol	946 mL in 1 BOTTLE, PLASTIC	SOLUTION	946		8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
87010-002	ISOPROPYL RUBBING ALCOHOL (ISOPROPYL ALCOHOL) SOLUTION [HEALTHWELL]	8	Legacy NDC, 2 package rows	20201008_360da52e-a158-4333-bf34-71e54fe7a837.zip

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
87010-002	87010-002-16, 87010-002-32

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
dc48176e-61b6-44fb-9938-7d82f29f35f1			360da52e-a158-4333-bf34-71e54fe7a837	2020-10-07	Warnings	Exact identifier spl id: dc48176e-61b6-44fb-9938-7d82f29f35f1 spl set id: 360da52e-a158-4333-bf34-71e54fe7a837

Reported adverse events (FAERS/openFDA)#

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