FDA.reportPublic FDA data

Alcohol prep Pad

Manufacturer
Xuchang Zhende Surgical Dressing Co.,Ltd.
Effective date
2022-12-27
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:42:50

Label at a glance#

ProductALCOHOL PREP PAD- Isopropyl Alcohol Swab
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Dosage and administration

wipe injection site vigorously and discard

Storage and handling

Protect from freezing and avoid excessive heat.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION


For preparation of 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
▪on mucus membranes
▪on irritated skin

OTC - WHEN USING SECTION


Keep out of reach of children.
If swallowed, get medical help or contact a Poison Control Center right
away

OTC - STOP USE SECTION

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

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

Directions

DOSAGE & ADMINISTRATION SECTION


wipe injection site vigorously and discard

Other information

STORAGE AND HANDLING SECTION

Protect from freezing and avoid excessive heat.

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL


REF: KZDC120303, Size: Medium, 200 pcs in box, 20 boxes in carton box
NDC: 80244-002-01

m size inner labelm size inner label

m size outer labelm size outer label

REF: KZDC120307, Size:Large, 200 pcs in box, 20 boxes in carton box
NDC: 80244-002-02

l size inner labell size inner label

l size outer labell size outer label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80244-002-012022-04-01C16284748780-1d6a99b39-7ee5-a426-e053-dadaa90af4c2addb504c-a930-44ea-e053-2995a90a8497
80244-002-022022-04-01C16284748780-1d6a99b39-7ee5-a426-e053-dadaa90af4c2addb504c-a930-44ea-e053-2995a90a8497
80244-002-012022-01-28C16284748780-1d6a99b39-7ee5-a426-e053-dadaa90af4c2addb504c-a930-44ea-e053-2995a90a8497
80244-002-022022-01-28C16284748780-1d6a99b39-7ee5-a426-e053-dadaa90af4c2addb504c-a930-44ea-e053-2995a90a8497

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
80244-00280244-002-01, 80244-002-02, 80244-002-03

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
0e7b15f8-a493-fb08-e063-6294a90aa5ecaddb504c-a930-44ea-e053-2995a90a84972024-01-08WarningsExact identifier
spl set id: addb504c-a930-44ea-e053-2995a90a8497

Reported adverse events (FAERS/openFDA)#

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