BodyMed Alcohol Prep Pad

Manufacturer
Boxout, LLC
Effective date
2025-11-14
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:16:15

Label at a glance#

ProductBodyMed Alcohol Prep Pad
Active ingredientISOPROPYL ALCOHOL
Label structure11 sections

Indications and uses

For cleasing and disinfecting.

Dosage and administration

Wipe over the intended area and discard.

Storage and handling

Store at room temperature 15-30⁰C (59-86⁰F).

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol USP, 70% v/v

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USES

INTENDED USE OF THE DEVICE

For cleasing and disinfecting.

WARNINGS

WARNINGS SECTION

For external use.only. Flammable; keep away from filre or flame. Do not use in the eyes, on irritated skin, on mucus membrane, and/or with electrocautery procedures.

DIRECTIONS FOR USE

INSTRUCTIONS FOR USE SECTION

Wipe over the intended area and discard.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

Store at room temperature 15-30⁰C (59-86⁰F).

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Water

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to skin as needed
Discard after single use

Directions for use

INDICATIONS & USAGE SECTION

Wipe over the intended area and discard.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If accidentally swallowed, seek medical assistance or immediately contact a Poison Control Center.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BodyMed Alcohol Prep Pad 82308-001BodyMed Alcohol Prep Pad 82308-001

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN6
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD6
797544isopropyl alcohol 70 % Medicated PadSY6
797544isopropyl alcohol 70 % Topical ClothSY6
797544isopropyl alcohol 70 % Topical SwabSY6

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
82308-001-012024-12-05C16284748780-11030e364-fff6-111a-e063-dadaa90a10e2d30dce9c-8d12-4c71-e053-2995a90a1205
82308-001-012024-01-30C16284748780-11030e364-fff6-111a-e063-dadaa90a10e2d30dce9c-8d12-4c71-e053-2995a90a1205

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82308-001-01BodyMed Alcohol Prep Pad100 mL in 1 BOXSWAB1006

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
82308-00182308-001-01

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
BodyMed Alcohol Prep PadALCOHOL PREP PADBoxout, LLCd30dce9c-8d12-4c71-e053-2995a90a12052025-11-14WarningsExact identifier
ndc (package): 82308-001-01
ndc (product): 82308-001
ndc11 (package): 82308000101
spl id: 4391a16f-7ca3-68ba-e063-6394a90a4250
spl set id: d30dce9c-8d12-4c71-e053-2995a90a1205

Reported adverse events (FAERS/openFDA)#

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