FDA.reportPublic FDA data

ALCOH-WIPE

Manufacturer
Veltek Associates, Inc. | Diamond Wipes International, Inc.
Effective date
2025-12-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:21:50

Label at a glance#

ProductALCOH-WIPE
Active ingredientISOPROPYL ALCOHOL
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70%

OTC - PURPOSE SECTION

Antiseptic Cleanser

INDICATIONS & USAGE SECTION

Use For preparation of the skin prior to injection

WARNINGS SECTION

Flammable, keep away from fire or flame. For external use only.

OTC - DO NOT USE SECTION

Do not use in the eyes. Do not use with electrocautery procedures.

OTC - ASK DOCTOR SECTION

Stop and ask a doctor if irritation and redness develop. If condition persists, consult a doctor.

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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions Open pad by tearing across top dotted line.

Wipe injection site vigorously and discard.

OTHER SAFETY INFORMATION

Other Information Store at room temperature. Alternate Use: Cleaning of ancillary devices.

INACTIVE INGREDIENT SECTION

Purified Water

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of wipe packet frontimage of wipe packet front

image of wipe packet backimage of wipe packet back

image of outer box_1image of outer box_1

image of outer box_2image of outer box_2

image of outer box_3image of outer box_3

image of outer box_4image of outer box_4

image of outer box_5image of outer box_5

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN2
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD2
797544isopropyl alcohol 70 % Medicated PadSY2
797544isopropyl alcohol 70 % Topical ClothSY2
797544isopropyl alcohol 70 % Topical SwabSY2

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64307-002-01ALCOH-WIPE1.03 mL in 1 PACKETSWAB1.032

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
64307-00264307-002-01

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-05-03monthly-update2026-06-03 17:38:38

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
ALCOH-WIPEISOPROPYL ALCOHOLVeltek Associates, Inc.343ba13e-7f90-5dab-e063-6294a90a56ae2025-12-10WarningsExact identifier
ndc (package): 64307-002-01
ndc (product): 64307-002
ndc11 (package): 64307000201
spl id: 459ea895-979a-b547-e063-6294a90a3443
spl set id: 343ba13e-7f90-5dab-e063-6294a90a56ae

Reported adverse events (FAERS/openFDA)#

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