Rubbing Alcohol 70% Isopropyl

Manufacturer
ZECO, LLC
Effective date
2024-03-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:07:39

Label at a glance#

ProductRubbing Alcohol 70% Isopropyl
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Storage and handling

Store at room temperature.  Avoid freezing and excessive heat above 40 ​° C (104 ​° F). Does not contain, nor is intended as a substitute for grain or ethyl alcohol.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v

OTC - PURPOSE SECTION

First Aid Antiseptic

INDICATIONS & USAGE SECTION

First aid to help reduce the risk of infection in minor cuts, scrapes and burns

OTC - ASK DOCTOR SECTION

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

WARNINGS SECTION

For external use only.

If taken internally, serious gastric disturbance will result.

Flammable, keep away from heat, sparks, flames, or hot surfaces.

When using this product, keep out of eyes, ears, and mouth.  If swallowed, get medical help or contact a Poison Control Center immediately.  In case of eye contact, immediately flush eyes thoroughly with water and seek medical advice.

Do not smoke while applying this product.

Ground/bond container and receiving equipment.

Use explosion-proof electrical/ventilating/lighting equipment.

Take precautionary measures against static discharge.

OTC - STOP USE SECTION

Stop using and ask a doctor if irritation or rash appears and lasts.  These may be a sign of a serious condition.

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.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS

  • Clean affected area.  Apply small amount of this product on the area 1-3 times daily.  If bandaged, let dry first.  May be covered with a sterile bandage.
  • Do not apply over large areas of the body.  Do not use longer than one week unless directed by doctor.

STORAGE AND HANDLING SECTION

Store at room temperature.  Avoid freezing and excessive heat above 40 ​°C (104 ​°F).

Does not contain, nor is intended as a substitute for grain or ethyl alcohol.

INACTIVE INGREDIENT SECTION

Purified Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3.78L NDC: 77093-300-01

18.92L NDC: 77093-300-02

208.19L NDC: 77093-300-03

1040.98L NDC: 77093-300-04

1249.19L NDC: 77093-300-05

image descriptionimage description

Add image transcription here...

FDA-Initiated Inactive NDC Indexing#

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
86161-30086161-300-01, 86161-300-02, 86161-300-03, 86161-300-04, 86161-300-05, 86161-300-06

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
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302ACTIB

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
212cbeec-cd91-bc8d-e063-6294a90aeaa41c50afa6-fff8-40f0-88fb-7b2fbaadc2c62024-08-01WarningsExact identifier
spl set id: 1c50afa6-fff8-40f0-88fb-7b2fbaadc2c6

Reported adverse events (FAERS/openFDA)#

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