Alcohol Prep Pad Medium

Manufacturer: Yangzhou Huanrui Medical Technology Co., Ltd
Effective date: 2026-09-08
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: daily-update
Hydrated at: 2026-09-12 01:01:14

Label at a glance#

ProductAlcohol Prep Pad Medium

Active ingredientISOPROPYL ALCOHOL

Label structure6 sections

Indications and uses

For preparation of 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

DOSAGE & ADMINISTRATION SECTION

For preparation of skin prior to injection

Warnings

WARNINGS SECTION

Flammable - keep away from fire or flame.

For external use only.

Flammable, keep away from fire or flame.

WARNINGS AND PRECAUTIONS SECTION

Do Not Use

OTC - DO NOT USE SECTION

with electrocautery procedures
In the eyes

Stop Use

OTC - STOP USE SECTION

If Irritation or redness develops.

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

INDICATIONS & USAGE SECTION

wipe injection site vigorously and discard

Inactive Ingredients

INACTIVE INGREDIENT SECTION

purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol Pad LabelAlcohol Prep Pad Label

Products#

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

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

Alcohol Prep Pad Medium
Alcohol Prep Pad
ISOPROPYL ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
87993-101	87993-101-00, 87993-101-01

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
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
WATER	059QF0KO0R	IACT

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
Alcohol Prep Pad Medium	ALCOHOL PREP PAD	Yangzhou Huanrui Medical Technology Co., Ltd	5af3eedc-d01e-c9e9-e063-6394a90a49e1	2026-09-08	Warnings	Exact identifier ndc (package): 87993-101-00 ndc (package): 87993-101-01 ndc (product): 87993-101 ndc11 (package): 87993010101 ndc11 (package): 87993010100 spl id: 5af3eeea-0568-dd24-e063-6294a90aaf66 spl set id: 5af3eedc-d01e-c9e9-e063-6394a90a49e1

Reported adverse events (FAERS/openFDA)#

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