FDA.reportPublic FDA data

Alcohol Prep Pad

Manufacturer
BioMed Resource Inc. | Shandong Haiyan Medical Manufacture Co. Ltd.
Effective date
2024-01-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 00:06:57

Label at a glance#

ProductAlcohol Prep Pad
Active ingredientIsopropyl Alcohol
Label structure9 sections

Label contents#

Full prescribing information#

Alcohol Prep Pad

OTC - ACTIVE INGREDIENT SECTION

70% Isoprppyl Alcohol

OTC - PURPOSE SECTION

Antispectic. For preparation of skin prior of injection.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, contact your phisician or Poison Control Center right away.

OTC - DO NOT USE SECTION

Do not use with electrocautery procedures.

INACTIVE INGREDIENT SECTION

Purified water.

DOSAGE & ADMINISTRATION SECTION

One piece at the time, Discard after use.

INDICATIONS & USAGE SECTION

Wipe injection site vigorously.Discard after use.

WARNINGS SECTION

1. For external use only;

2. Flammable. Keep away from heat or flame;

3. Aviod to contact eyes. Flush throoughly with water in case of contact;

4. Stop use if irritation or redness develop;

5. Do not use with electrocautery procedures;

Keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol Prep PadAlcohol Prep Pad

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69250-661-022022-03-18C16284748780-19d75b9d0-e90b-f424-e053-dadaa90a57ceAlcohol Prep pad
69250-661-022022-01-28C16284748780-19d75b9d0-e90b-f424-e053-dadaa90a57ceAlcohol Prep pad
69250-661-022020-05-10C16284748780-19d75b9d0-e90b-f424-e053-dadaa90a57ceAlcohol Prep pad
69250-661-022020-01-31C16284748780-19d75b9d0-e90b-f424-e053-dadaa90a57ceAlcohol Prep pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69250-661-02Alcohol Prep Pad200 mL in 1 BOXSPONGE2004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69250-661ALCOHOL PREP PAD SPONGE [BIOMED RESOURCE INC.]4Current NDC, Legacy NDC, 1 package rows20240111_03be8a96-c163-0e22-e054-00144ff8d46c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Isopropyl AlcoholACTIVE INGREDIENTND2M4163021
Isopropyl AlcoholACTIVE MOIETYND2M4163021
waterINACTIVE INGREDIENT059QF0KO0R1

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
69250-66169250-661-02

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
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
Alcohol Prep PadALCOHOL PREP PADBioMed Resource Inc.03be8a96-c163-0e22-e054-00144ff8d46c2024-01-10WarningsExact identifier
ndc (package): 69250-661-02
ndc (product): 69250-661
ndc11 (package): 69250066102
spl id: 0e9d506d-8c0f-ab6b-e063-6294a90a5ab6
spl set id: 03be8a96-c163-0e22-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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