BIOPURE 70% Isopropyl Alcohol Wipe

Manufacturer: QUEST USA CORP
Effective date: 2026-07-19
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: daily-update
Hydrated at: 2026-07-21 05:10:18

Label at a glance#

ProductBiopure 70% Isopropyl Alcohol Wipe

Active ingredientISOPROPYL ALCOHOL

Label structure9 sections

Indications and uses

First aid to help prevent infection in minor cuts, scrapes, and burns.

Dosage and administration

Clean the affected area. Apply product on the affected area of the body 1 to 3 times a day. The affected area could be covered with a sterile bandage. If bandaged, let dry first. Discard after use.

Storage and handling

For external use only. Keep the lid tightly closed and store at room temperature. Hold away from face when opening.

Contacts and useful links#

PhoneLabel contact800-292-2417

Label contents#

Full prescribing information#

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 infection in minor cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

OTC - ASK DOCTOR SECTION

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

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.

OTC - STOP USE SECTION

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

OTC - DO NOT USE SECTION

do not use in or near the eyes
do not apply over large areas
do not use longer than 1 week unless directed by a doctor.

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected area. Apply product on the affected area of the body 1 to 3 times a day. The affected area could be covered with a sterile bandage. If bandaged, let dry first. Discard after use.

Other information

STORAGE AND HANDLING SECTION

For external use only. Keep the lid tightly closed and store at room temperature. Hold away from face when opening.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water

Questions?

OTC - QUESTIONS SECTION

Call 800-292-2417

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

IPA Wipe LabelIPA Wipe Label

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0198926007859	GTIN-13: 0198926007859 EAN-13: 0198926007859 GTIN-12: 198926007859 UPC-A: 198926007859 GTIN storage (14 digits): 00198926007859	IPA Wipe1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1	Product name	1	20230829

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Biopure 70% Isopropyl Alcohol Wipe
Isopropyl Alcohol, Wipe
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78691-030	78691-030-01

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
1	2025-07-21	full-release	2026-06-01 01:10:32

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
Biopure 70% Isopropyl Alcohol Wipe	ISOPROPYL ALCOHOL, WIPE	QUEST USA CORP	3a7932c4-6f90-a008-e063-6294a90aa769	2026-07-19	Warnings	Exact identifier ndc (package): 78691-030-01 ndc (product): 78691-030 ndc11 (package): 78691003001 spl id: 56faf191-a790-ef51-e063-6294a90afe83 spl set id: 3a7932c4-6f90-a008-e063-6294a90aa769

Reported adverse events (FAERS/openFDA)#

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