FDA.reportPublic FDA data

Alcohol Prep Pad

Manufacturer
Caribbean Medical Brokers | Specialty Medical Supplies Beijing Co., Ltd.
Effective date
2010-03-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 22:23:57

Label at a glance#

ProductAlcohol Prep Pad
Active ingredientIsopropyl Alcohol
Label structure12 sections

Storage and handling

Other information:   Store at room temperature.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:

Isopropyl Alcohol USP, 70% v/v

OTC - PURPOSE SECTION

Purpose

Antiseptic

INDICATIONS & USAGE SECTION

Use:  For preparation of skin prior to an injection to decrease germs in minor cuts and scrapes.

WARNINGS SECTION

Warnings:  For external use only.

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.

GENERAL PRECAUTIONS SECTION

Caution:  Do not apply to irritated skin.

OTC - DO NOT USE SECTION

Do not use in the eyes or on mucous membranes.  In case of deep or puncture wounds, consult a doctor.

DOSAGE & ADMINISTRATION SECTION

Directions:  Wipe injection site vigorously.

STORAGE AND HANDLING SECTION

Other information:  Store at room temperature.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:  Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100 Individual Pads

NDC: 68113-996-01

Alcohol Prep Pads

Antiseptic for preparation of the skin prior to injection

For Individual, Professional, and Hospital Use

Saturated with 70% v/v Isopropyl Alcohol for external use only

SMS Alcohol Prep Pad Labeling

SMS Alcohol Prep Pad LabelingSMS Alcohol Prep Pad Labeling

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68113-996-012019-10-21C16284748780-1956f9ecf-cf1b-621f-e053-dbdaa90a74adAlcohol Prep Pad
68113-996-022019-10-21C16284748780-1956f9ecf-cf1b-621f-e053-dbdaa90a74adAlcohol Prep Pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68113-996-01Alcohol Prep Pad70 mL in 1 POUCHLIQUID704
68113-996-01Alcohol Prep Pad100 in 1 BOXLIQUID1004
68113-996-02Alcohol Prep Pad200 in 1 BOXLIQUID2004
68113-996-02Alcohol Prep Pad70 mL in 1 POUCHLIQUID704

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68113-996ALCOHOL PREP PAD LIQUID [CARIBBEAN MEDICAL BROKERS]4Legacy NDC, 4 package rows20100323_9a6dd21b-d11d-4241-8584-7c92167df9b1.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68113-996-01EA - Each68113-9960735d1bf-b28f-4652-baf4-4a22b0ec60b312012-07-24
68113-996-02EA - Each68113-9960eb92fca-61d3-4a59-ad84-d905ab10dcc912024-04-05

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Isopropyl AlcoholACTIVE INGREDIENTND2M4163024
Isopropyl AlcoholACTIVE MOIETYND2M4163024
WaterINACTIVE INGREDIENT059QF0KO0R4

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
68113-99668113-996-01, 68113-996-02

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
Isopropyl AlcoholND2M416302ACTIB
Water059QF0KO0RIACT

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
5d7947ab-f60d-499d-84dd-bddd949caf789a6dd21b-d11d-4241-8584-7c92167df9b12010-03-19WarningsExact identifier
spl id: 5d7947ab-f60d-499d-84dd-bddd949caf78
spl set id: 9a6dd21b-d11d-4241-8584-7c92167df9b1

Reported adverse events (FAERS/openFDA)#

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