UNIVERSAL ISOPROPYL RUBBING ALCOHOL 70% - isopropyl alcohol liquid

Manufacturer: TSM BRANDS LLC | TSM BRANDS KIMYA SANAYI VE DIS TICARET ANONIM SIRKETI
Effective date: 2025-06-30
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:06:28

Label at a glance#

ProductUNIVERSAL ISOPROPYL RUBBING ALCOHOL 70% - isopropyl alcohol liquid

Active ingredientISOPROPYL ALCOHOL

Label structure12 sections

Indications and uses

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

Dosage and administration

clean effected area apply small amount of this product on the area 1-3 times daily May be covered with a sterile bandage If bandaged, let dry firs

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

Deep punctured wounds, animal bites or serious burns

Stop using this product if

OTC - DO NOT USE SECTION

conditions persists or gets worse

Keep this and all drugs out of reach of the children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek professional assistance or contact a Poison control control center ( 1-800-222-1222) immediately

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Stop using this product if

OTC - STOP USE SECTION

condition persist or gets worse

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 one week unless directed by a doctor

Warnngs

WARNINGS SECTION

For external use only, flammable, keep away from fire or flammable, heat, spark, electrical

Directions

DOSAGE & ADMINISTRATION SECTION

clean effected area

apply small amount of this product on the area 1-3 times daily

May be covered with a sterile bandage

If bandaged, let dry firs

Inactive Ingredient

INACTIVE INGREDIENT SECTION

purified water

Uses

INDICATIONS & USAGE SECTION

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

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BACK LABELFRONT LABEL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
808520	isopropyl alcohol 70 % Topical Solution	PSN	1
808520	isopropyl alcohol 0.7 ML/ML Topical Solution	SCD	1
808520	isopropyl alcohol 70 % Topical Solution	SY	1

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
76567-4301-6	UNIVERSAL ISOPROPYL RUBBING ALCOHOL 70% - isopropyl alcohol liquid	473 mL in 1 BOTTLE, PLASTIC	LIQUID	473		1

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 liquid
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76567-4301	76567-4301-6

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 liquid	UNIVERSAL ISOPROPYL RUBBING ALCOHOL 70% - ISOPROPYL ALCOHOL LIQUID	TSM BRANDS LLC	38d03665-6e76-c76f-e063-6294a90a9e33	2025-06-30	Warnings	Exact identifier ndc (package): 76567-4301-6 ndc (product): 76567-4301 ndc11 (package): 76567430106 spl id: 38d03665-6e77-c76f-e063-6294a90a9e33 spl set id: 38d03665-6e76-c76f-e063-6294a90a9e33

Reported adverse events (FAERS/openFDA)#

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