The Pharma-C Company 70 Isopropyl Alcohol Wipes

Manufacturer
Kleen Test Products Corporation
Effective date
2025-06-04
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 01:02:13

Label at a glance#

ProductThe Pharma-C Company 70 Isopropyl Alcohol Wipes
Active ingredientISOPROPYL ALCOHOL
Label structure9 sections

Indications and uses

first aid to help prevent the risk of infection in: • minor cuts • scrapes • burns

Dosage and administration

• clean the affected area • apply product on the affected area of the body 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of infection in:

• minor cuts • scrapes • burns

Warnings

WARNINGS SECTION

For external use only.

Flammablekeep away from fire or flame, heat, spark, electrical 

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

• deep or puncture wounds • animal bites • serious burns

When using this product

OTC - WHEN USING SECTION

• do not get in eyes • do not apply over large areas of the body • do not use longer than 1 week unless directed by a doctor

Stop use and ask doctor 

OTC - STOP USE SECTION

if condition persists or gets worse.

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

• clean the affected area • apply product on the affected area of the body 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

Other information

SPL UNCLASSIFIED SECTION

• do not apply internally • keep canister tightly closed and stored at room temperature • hold away from face when opening

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-844-308-8600

Package Labeling: (40 Count)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label03Label03

Package Labeling: (175 Count)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label02Label02

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797544isopropyl alcohol 70 % Medicated PadPSN8
797544isopropyl alcohol 0.7 ML/ML Medicated PadSCD8
797544isopropyl alcohol 70 % Medicated PadSY8
797544isopropyl alcohol 70 % Topical ClothSY8
797544isopropyl alcohol 70 % Topical SwabSY8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55239-362-00The Pharma-C Company 70 Isopropyl Alcohol Wipes4.5 mL in 1 PATCHCLOTH4.58
55239-362-00The Pharma-C Company 70 Isopropyl Alcohol Wipes40 in 1 CANISTERCLOTH408
55239-362-01The Pharma-C Company 70 Isopropyl Alcohol Wipes175 in 1 CANISTERCLOTH1758
55239-362-01The Pharma-C Company 70 Isopropyl Alcohol Wipes5.2 mL in 1 PATCHCLOTH5.28

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
55239-36255239-362-00, 55239-362-01

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
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
The Pharma-C Company 70 Isopropyl Alcohol WipesISOPROPYL ALCOHOLKleen Test Products Corporationa0f93dac-7baa-4f79-b6a0-3cabe52806bb2025-06-04WarningsExact identifier
ndc (package): 55239-362-01
ndc (package): 55239-362-00
ndc (product): 55239-362
ndc11 (package): 55239036200
ndc11 (package): 55239036201
spl id: 36942dea-6578-2075-e063-6294a90a70af
spl set id: a0f93dac-7baa-4f79-b6a0-3cabe52806bb

Reported adverse events (FAERS/openFDA)#

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