Quality Choice Hydrogen Peroxide Wipes

Manufacturer
Chain Drug Marketing Association, Inc | Kleen Test Products Corporation
Effective date
2025-05-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:01:34

Label at a glance#

ProductQuality Choice Hydrogen Peroxide Wipes
Active ingredientHYDROGEN PEROXIDE
Label structure8 sections

Indications and uses

first aid to help reduce 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

Hydrogen peroxide (stabilized) 3%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

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

Warnings

WARNINGS SECTION

For external use only.

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

• do not use longer than 1 week unless directed by a doctor

Stop use and ask doctor if

OTC - STOP USE SECTION

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

polysorbate 80, purified water

Questions or comments?

OTC - QUESTIONS SECTION

1-800-935-2362

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label0Label0

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797811hydrogen peroxide 3 % Medicated PadPSN1
797811hydrogen peroxide 30 MG/ML Medicated PadSCD1
797811hydrogen peroxide 3 % Medicated PadSY1
797811hydrogen peroxide 3 % Topical SwabSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83324-290-40Quality Choice Hydrogen Peroxide Wipes40 in 1 CANISTERCLOTH401
83324-290-40Quality Choice Hydrogen Peroxide Wipes4.5 g in 1 APPLICATORCLOTH4.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83324-290QUALITY CHOICE HYDROGEN PEROXIDE WIPES (HYDROGEN PEROXIDE) CLOTH [CHAIN DRUG MARKETING ASSOCIATION, INC]1Current NDC, 2 package rows20250528_c2822eb6-8a2a-4337-acce-6f7fc8496175.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
83324-29083324-290-40

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYSORBATE 806OZP39ZG8HIACT
WATER059QF0KO0RIACT
HYDROGEN PEROXIDEBBX060AN9VACTIB

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
Quality Choice Hydrogen Peroxide WipesHYDROGEN PEROXIDEChain Drug Marketing Association, Incc2822eb6-8a2a-4337-acce-6f7fc84961752025-05-26WarningsExact identifier
ndc (package): 83324-290-40
ndc (product): 83324-290
ndc11 (package): 83324029040
spl id: 35a2492e-9326-799d-e063-6294a90aa045
spl set id: c2822eb6-8a2a-4337-acce-6f7fc8496175

Reported adverse events (FAERS/openFDA)#

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