99.9% Isopropyl Alcohol

Manufacturer
Belle Chemical LLC
Effective date
2024-01-14
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:14:25

Label at a glance#

Product99.9% Isopropyl Alcohol
Active ingredientISOPROPYL ALCOHOL
Label structure13 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 99.9%

OTC - PURPOSE SECTION

First Aid Antiseptic

WARNINGS SECTION

For external use only. If taken internally serious gastric disturbances will result.

Flammable keep away from fire or flame, heat, spark, electrical.

Caution – Fumes can be acutely irritating to skin, eyes and the respiratory system. Do not apply to irritated skin or if excessive irritation develops. Avoid getting into the eyes or on mucous membranes. Avoid inhaling this product.

OTC - ASK DOCTOR SECTION

Ask a doctor before use for deep or puncture wounds, animal bites or serious burns

OTC - WHEN USING SECTION

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 1 week

OTC - STOP USE SECTION

Stop use and ask 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 right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • clean the 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

INDICATIONS & USAGE SECTION

helps prevent the risk of infection in:

  • minor cuts
  • scrapes
  • burns

SPL UNCLASSIFIED SECTION

Other information:

  • does not contain, nor is intended as a substitute for grain or ethyl alcohol

INACTIVE INGREDIENT SECTION

Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

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
82771-99982771-999-32

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
339d084d-ea7f-7b22-e063-6394a90adfe9eaeb310d-ace6-4489-e053-2995a90a42522025-04-25WarningsExact identifier
spl set id: eaeb310d-ace6-4489-e053-2995a90a4252

Reported adverse events (FAERS/openFDA)#

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