Universal ISOPROPYL Rubbing Alcohol 70%

Manufacturer: Universal Distribution Center LLC
Effective date: 2026-02-10
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-06-01 01:47:03

Label at a glance#

ProductUniversal ISOPROPYL Rubbing Alcohol 70%

Active ingredientISOPROPYL ALCOHOL

Label structure9 sections

Indications and uses

• first aid to help prevent the risk of infection in minor cuts, scrapes and burns.

Dosage and administration

• clean the affected area • apply small amount of product on the affected area 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

Storage and handling

• store at controlled room temperature • does not contain, nor is intended as a substitute for grain or ethyl alcohol

Contacts and useful links#

PhonePoison Help1-800-222-1222

Websitewww.universaldc.com

www.universaldc.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

first aid antiseptic

Uses:

INDICATIONS & USAGE SECTION

• first aid to help prevent the risk of infection in minor cuts, scrapes and burns.

Warnings:

WARNINGS SECTION

For external use only.

• if taken internally, serious gastric disturbances will occur
• flammable, keep away from fire or flame, heat, spark, electrical
• use only in a well-ventilated area; fumes may be toxic

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

When using this product • do not get into eyes • do not inhale • do not apply over large areas of the body • do not use longer than one week unless directed by a doctor

Stop use and ask a doctor if condition persists or gets worse

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. 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 • apply small amount of product on the affected area 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

Other Information

STORAGE AND HANDLING SECTION

• store at controlled room temperature
• does not contain, nor is intended as a substitute for grain or ethyl alcohol

Inactive Ingredient:

INACTIVE INGREDIENT SECTION

Purified Water

SPL UNCLASSIFIED SECTION

For Rubbing & Massaging

Use only in a well-ventilated area.
Fumes may be harmful.

TAMPER EVIDENT: DO NOT USE IF THE PRINTED SAFETY FOIL UNDER THE CAP IS BROKEN OR MISSING.

Made in Turkey

Mfd for and Distributed By:
Universal Distribution Center LLC
330 Applegarth Road, Monroe Township, NJ 08831
www.universaldc.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RUBBING ALCOHOL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
808520	isopropyl alcohol 70 % Topical Solution	PSN	2
808520	isopropyl alcohol 0.7 ML/ML Topical Solution	SCD	2
808520	isopropyl alcohol 70 % Topical Solution	SY	2

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0676979860084	GTIN-13: 0676979860084 EAN-13: 0676979860084 GTIN-12: 676979860084 UPC-A: 676979860084 GTIN storage (14 digits): 00676979860084	52000430-5.jpg
Barcode	EAN-13	0676979860831	GTIN-13: 0676979860831 EAN-13: 0676979860831 GTIN-12: 676979860831 UPC-A: 676979860831 GTIN storage (14 digits): 00676979860831	52000430-5.jpg

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
52000-430-12	Universal ISOPROPYL Rubbing Alcohol 70%	355 mL in 1 BOTTLE, PLASTIC	LIQUID	355		2
52000-430-16	Universal ISOPROPYL Rubbing Alcohol 70%	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473		2

Products#

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

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

Universal ISOPROPYL Rubbing Alcohol 70%
Isopropyl alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52000-430	52000-430-16, 52000-430-12

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
Universal ISOPROPYL Rubbing Alcohol 70%	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	0c76f14b-9a0c-4573-96f2-cd4080eb99e6	2026-02-10	Warnings	Exact identifier ndc (package): 52000-430-12 ndc (package): 52000-430-16 ndc (product): 52000-430 ndc11 (package): 52000043016 ndc11 (package): 52000043012 spl id: 1f9eaaed-f62e-4e0d-b188-0f44da1c7f6e spl set id: 0c76f14b-9a0c-4573-96f2-cd4080eb99e6

Reported adverse events (FAERS/openFDA)#

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