Alcohol Cleansing

Manufacturer
CMC Group Inc.
Effective date
2025-01-13
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:52:44

Label at a glance#

ProductAlcohol Cleansing
Active ingredientISOPROPYL ALCOHOL
Label structure7 sections

Dosage and administration

Wipe injection site vigorously and discard.

Label contents#

Full prescribing information#

Active Ingredient:

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol, 70% v/v

Purpose:

OTC - PURPOSE SECTION

Antiseptic

Use:

INDICATIONS & USAGE SECTION

For preparation of the skin before 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, in the eyes

Stop use

OTC - STOP USE SECTION

if irritation and redness develop. If condition persists for more than 72 hours, consult your doctor.

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 site vigorously and discard.

Other information:

SPL UNCLASSIFIED SECTION

Store at room temperature 15°-30° C (59°-86° F)

Inactive ingredient:

INACTIVE INGREDIENT SECTION

Purified water.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Alcohol cleansingAlcohol cleansing

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN5
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD5
797544isopropyl alcohol 70 % Medicated PadSY5
797544isopropyl alcohol 70 % Topical ClothSY5
797544isopropyl alcohol 70 % Topical SwabSY5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49687-0012-02025-01-14C16284748780-11030e365-1825-111a-e063-dadaa90a10e2Alcohol Cleansing Pads
49687-0012-02024-01-30C16284748780-11030e365-1825-111a-e063-dadaa90a10e2Alcohol Cleansing Pads

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49687-0012-0Alcohol Cleansing0.9 g in 1 POUCHCLOTH0.95
49687-0012-0Alcohol Cleansing20 in 1 KITCLOTH205

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49687-0012ALCOHOL CLEANSING (ISOPROPYL ALCOHOL) CLOTH [CMC GROUP INC.]5Current NDC, Legacy NDC, 2 package rows20250116_e3985ef1-503a-4193-a5b5-7910aefa7814.zip

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
49687-001249687-0012-0

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 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Standard ANSI First AidWATER, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, LIDOCAINE HYDROCHLORIDECMC Group, Inc.e1ef74bf-8895-4200-a411-f726dcdaa9452025-04-02WarningsExact identifier
ndc (package): 49687-0012-0
ndc11 (package): 49687001200
Large ANSI First Aid KitWATER, BENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL, BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, LIDOCAINE HYDROCHLORIDECMC Group, Inc.fa8578c2-a0bc-4e2e-a4f9-d48debfff3782025-04-02WarningsExact identifier
ndc (package): 49687-0012-0
ndc11 (package): 49687001200
Alcohol CleansingISOPROPYL ALCOHOLCMC Group Inc.e3985ef1-503a-4193-a5b5-7910aefa78142025-01-13WarningsExact identifier
ndc (package): 49687-0012-0
ndc (product): 49687-0012
ndc11 (package): 49687001200
spl id: 2b9b3edf-5b7d-9898-e063-6294a90a7158
spl set id: e3985ef1-503a-4193-a5b5-7910aefa7814

Reported adverse events (FAERS/openFDA)#

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