ISOPROPYL ALCOHOL 70%

Manufacturer
INDUSTRY SUPPLY INC | Vedco
Effective date
2021-04-16
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:46:47

Label at a glance#

ProductISOPROPYL ALCOHOL 70%
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Storage and handling

Does not contain, nor is inteded as a subsitutire for grain or ethyl alcohol. Will produce serious gastric disturbances if taken internally. Protect from freezing and avoid excessive heat.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

This is Isopropyl Alcohol 70% USP.

We are just relabeling this product.

It is made with only the following:

Isopropyl Alcohol USP or Food Chemical Codex (FCC) Grade) 70% Volume/Volume

Sterile, distilled, or boiled cold water

The firm does not add other active or inactive ingredients. Different or additonal ingredients may impace the quality and potency of the product.

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v Purpose:Antiseptic

OTC - PURPOSE SECTION

Antiseptic: For first adi to help prevent the risk of infection in minor cuts, scrapes, or burns.

INDICATIONS & USAGE SECTION

For First Aid to help prevent the risk of infection in minor cuts, scrapes, and burns.

WARNINGS SECTION

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

OTC - WHEN USING SECTION

When using this product do not get into eyes, apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition persists or gets worse or lasts for for more than 72 hours. Do not use longer than 1 week unless directed by a doctor.

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.

DOSAGE & ADMINISTRATION SECTION

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

STORAGE AND HANDLING SECTION

Does not contain, nor is inteded as a subsitutire for grain or ethyl alcohol. Will produce serious gastric disturbances if taken internally. Protect from freezing and avoid excessive heat.

INACTIVE INGREDIENT SECTION

Purified Water USP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AEC IPA 32 OZ.AEC IPA 32 OZ.

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50989-30950989-309-27

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
NameUNIIKind
ISOPROPYL ALCOHOLND2M416302ACTIB
WATER059QF0KO0RIACT

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c199c182-649e-96be-e053-2995a90adc5bc01b025e-70a2-4907-e053-2995a90a99bf2021-05-05WarningsExact identifier
spl set id: c01b025e-70a2-4907-e053-2995a90a99bf

Reported adverse events (FAERS/openFDA)#

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