Alcohol Pad

Manufacturer: LaMi Products INC.
Effective date: 2023-10-19
Label type: HUMAN OTC DRUG LABEL
Version: 5
Source: legacy-cache
Hydrated at: 2026-08-01 21:23:53

Label at a glance#

ProductAlcohol Pad

Active ingredientISOPROPYL ALCOHOL

Label structure6 sections

Indications and uses

Preparation of the skin prior to injection

Dosage and administration

wipe injection site vigorously and discard

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol, 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

Preparation of the skin prior to injection

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire of flame.

Do not use

OTC - DO NOT USE SECTION

with electrocautery procedures
in the eyes.

Stop use

OTC - STOP USE SECTION

If irritation or redness develop. If the condition persists for more than 72 hours, consult a doctor.

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 site vigorously and discard

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label

Products#

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

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

Alcohol Pad
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70430-001	70430-001-01

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
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
2f2ef71b-0560-b7a3-e063-6394a90a3d89			f3d152f3-77a9-4e52-9e79-e27ce589005f	2025-02-28	Warnings	Exact identifier spl set id: f3d152f3-77a9-4e52-9e79-e27ce589005f

Reported adverse events (FAERS/openFDA)#

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