Alcohol Prep

Manufacturer
Geri-Gentle Corporation
Effective date
2023-11-10
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
legacy-cache
Hydrated at
2026-08-01 21:21:09

Label at a glance#

ProductAlcohol Prep
Active ingredientISOPROPYL ALCOHOL
Label structure7 sections

Dosage and administration

Wipe injection area and discard.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For preparation of the skin prior to injection.

Warnings

WARNINGS SECTION

  • For external use only.
  • Flammable, keep away from fire or flame.

Do Not Use

OTC - DO NOT USE SECTION

  • with electrocautery procedures.
  • In the eyes. If contact occurs, flush eyes with water.

Stop Use

OTC - STOP USE SECTION

If irritation and redness develop. If condition continues, consult your health care practitioner.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed,get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wipe injection area and discard.

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature 15 C~30 C(59 F~86 F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

112233

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
69771-00369771-003-00

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
2a9fb0bb-65d2-e313-e063-6394a90abf30bdd1ed40-ce09-4cca-bee5-ddb86ede4d1f2025-01-01WarningsExact identifier
spl set id: bdd1ed40-ce09-4cca-bee5-ddb86ede4d1f

Reported adverse events (FAERS/openFDA)#

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