FDA.reportPublic FDA data

70% ISOPROPYL ALCOHOL PREP PAD

Manufacturer
Landy International | Zhangzhou Zhongnan Nursing Products Co.,ltd
Effective date
2020-12-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:36:12

Label at a glance#

Product70% ISOPROPYL ALCOHOL PREP PAD
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

Dosage and administration

Wipe over the skin or affected area, recommended for single use, dispose of used wipe in an approved manner.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: Isopropyl Alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

USES: Sterile antiseptic wipe, recommended for single use.

Warnings

WARNINGS SECTION

FLAMMABLE. Keep away from fire, electrical & spark
For external use only. Do not use In ears, eyes or mouth.
●Avoid contact with the eyes. In case of contact, flush eyes with water
●Stop use and ask a doctor if redness or iritation develop
●If swallowed contact a poison center

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

Directions

DOSAGE & ADMINISTRATION SECTION

Wipe over the skin or affected area, recommended for single use, dispose of used wipe in an approved manner.

Inactive ingredients

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Chlorphenesin, Purified Water,
Propylene Glycol

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11223344

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN1
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD1
797544isopropyl alcohol 70 % Medicated PadSY1
797544isopropyl alcohol 70 % Topical ClothSY1
797544isopropyl alcohol 70 % Topical SwabSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51706-963-012021-07-23C16284748780-1c7ccaba7-23eb-fd44-e053-dadaa90aa01b51706-963 70% ISOPROPYL ALCOHOL PREP PAD
51706-963-022021-07-23C16284748780-1c7ccaba7-23eb-fd44-e053-dadaa90aa01b51706-963 70% ISOPROPYL ALCOHOL PREP PAD

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51706-963-0170% ISOPROPYL ALCOHOL PREP PAD1 in 1 BAGCLOTH11
51706-963-0170% ISOPROPYL ALCOHOL PREP PAD2.33 g in 1 NOT APPLICABLECLOTH2.331
51706-963-0270% ISOPROPYL ALCOHOL PREP PAD0.238 g in 1 NOT APPLICABLECLOTH0.2381
51706-963-0270% ISOPROPYL ALCOHOL PREP PAD1 in 1 BAGCLOTH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51706-96370% ISOPROPYL ALCOHOL PREP PAD (ISOPROPYL ALCOHOL) CLOTH [LANDY INTERNATIONAL]1Legacy NDC, 4 package rows20201231_b7acb0d6-d062-c2f9-e053-2995a90a925b.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51706-96351706-963-01, 51706-963-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLORPHENESINI670DAL4SZIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
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
b7acb118-6b9a-7c87-e053-2995a90add57b7acb0d6-d062-c2f9-e053-2995a90a925b2020-12-30WarningsExact identifier
spl id: b7acb118-6b9a-7c87-e053-2995a90add57
spl set id: b7acb0d6-d062-c2f9-e053-2995a90a925b

Reported adverse events (FAERS/openFDA)#

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