FDA.reportPublic FDA data

Alcohol Pad

Manufacturer
Redicare LLC
Effective date
2019-12-11
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:01:58

Label at a glance#

ProductAlcohol Pad
Active ingredientISOPROPYL ALCOHOL
Label structure7 sections

Dosage and administration

Wipe injection area and discard.

Label contents#

Full prescribing information#

Active Ingredient (in each towelette) ............Purpose

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%..........Antiseptic

Use:

OTC - PURPOSE 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

Stop use if

OTC - STOP USE SECTION

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

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:

DOSAGE & ADMINISTRATION SECTION

Wipe injection area and discard.

Other information:

INDICATIONS & USAGE SECTION

Store at room temperature 15 o to 30 oC (59 o to 86 oF).

Inactive ingredient:

INACTIVE INGREDIENT SECTION

water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BoxBoxPacketPacket

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN4
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD4
797544isopropyl alcohol 70 % Medicated PadSY4
797544isopropyl alcohol 70 % Topical ClothSY4
797544isopropyl alcohol 70 % Topical SwabSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71105-111-032020-09-27C16284748780-1ab0e2407-3566-f274-e053-dbdaa90a6471Alcohol Prep Pads
71105-111-032020-09-25C16284748780-1ab0e2407-3566-f274-e053-dbdaa90a6471Alcohol Prep Pads
71105-111-032020-07-22C16284748780-1ab0e2407-3566-f274-e053-dbdaa90a6471Alcohol Prep Pads

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71105-111-01Alcohol Pad0.45 g in 1 PATCHSWAB0.454
71105-111-02Alcohol Pad1 in 1 PACKETSWAB14
71105-111-03Alcohol Pad50 in 1 BOXSWAB504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71105-111ALCOHOL PAD (ALCOHOL PREP PAD) SWAB [REDICARE LLC]4Legacy NDC, 3 package rows20191212_46eb8e9a-4513-5739-e054-00144ff88e88.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71105-11171105-111-01, 71105-111-02, 71105-111-03

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
99734a37-c2f0-47b4-e053-2995a90a0d4f46eb8e9a-4513-5739-e054-00144ff88e882019-12-11WarningsExact identifier
spl id: 99734a37-c2f0-47b4-e053-2995a90a0d4f
spl set id: 46eb8e9a-4513-5739-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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