Universal Rubbing Alcohol

Manufacturer: Universal Distribution Center LLC
Effective date: 2026-02-23
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: full-release
Hydrated at: 2026-06-01 01:47:22

Label at a glance#

ProductUniversal Rubbing Alcohol

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 a 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#

Websitewww.universaldc.com

www.universaldc.com

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 91%

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 puncture 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 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 a 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

UniversalRubbingAlcohol

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
582901	isopropyl alcohol 91 % Topical Solution	PSN	5
582901	isopropyl alcohol 0.91 ML/ML Topical Solution	SCD	5
582901	isopropyl alcohol 91 % Topical Solution	SY	5

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0676979555973	GTIN-13: 0676979555973 EAN-13: 0676979555973 GTIN-12: 676979555973 UPC-A: 676979555973 GTIN storage (14 digits): 00676979555973	52000406-7.jpg
Barcode	EAN-13	0676979555980	GTIN-13: 0676979555980 EAN-13: 0676979555980 GTIN-12: 676979555980 UPC-A: 676979555980 GTIN storage (14 digits): 00676979555980	52000406-7.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
52000-406-35	Universal Rubbing Alcohol	355 mL in 1 BOTTLE, PLASTIC	LIQUID	355		5
52000-406-36	Universal Rubbing Alcohol	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473		5

Products#

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

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

Universal Rubbing Alcohol
Isopropyl alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52000-406	52000-406-35, 52000-406-36

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

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
4	2025-11-19	monthly-update	2026-06-03 17:40:51

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 Rubbing Alcohol	ISOPROPYL ALCOHOL	Universal Distribution Center LLC	183efdc2-cf3e-4f06-b292-0cfd097418b3	2026-02-23	Warnings	Exact identifier ndc (package): 52000-406-36 ndc (package): 52000-406-35 ndc (product): 52000-406 ndc11 (package): 52000040636 ndc11 (package): 52000040635 spl id: 5c1ba88a-39ac-49b3-bfaa-d3e022a000ec spl set id: 183efdc2-cf3e-4f06-b292-0cfd097418b3

Reported adverse events (FAERS/openFDA)#

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