FDA.reportPublic FDA data

Quality Choice Hydrogen Peroxide Wipes

Manufacturer
Chain Drug Marketing Association, Inc.
Effective date
2026-01-09
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
monthly-update
Hydrated at
2026-06-03 17:51:39

Label at a glance#

ProductQuality Choice Hydrogen Peroxide Wipes
Active ingredientHYDROGEN PEROXIDE
Label structure7 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

Hydrogen peroxide (stabilized) 3%

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.

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

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 at controlled room temperature 
  • hold away from face when opening

Inactive ingredient

INACTIVE INGREDIENT SECTION

polysorbate 80, purified water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
797811hydrogen peroxide 3 % Medicated PadPSN3
797811hydrogen peroxide 30 MG/ML Medicated PadSCD3
797811hydrogen peroxide 3 % Medicated PadSY3
797811hydrogen peroxide 3 % Topical SwabSY3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63868-184-40Quality Choice Hydrogen Peroxide Wipes4.5 mL in 1 PATCHCLOTH4.53
63868-184-40Quality Choice Hydrogen Peroxide Wipes40 in 1 CANISTERCLOTH403

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63868-184-40EA - Each63868-1844f3acee1-017b-4a8e-8ac7-f21e160d3c3a12023-06-06

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
63868-18463868-184-40

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
HYDROGEN PEROXIDEBBX060AN9VACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22023-11-09full-release2026-05-31 23:59:44

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, Inc.b5815ca2-edaa-bc8c-e053-2a95a90a3df22026-01-09WarningsExact identifier
ndc (package): 63868-184-40
ndc (product): 63868-184
ndc11 (package): 63868018440
spl id: 47f65581-391b-a39e-e063-6394a90a7df2
spl set id: b5815ca2-edaa-bc8c-e053-2a95a90a3df2

Reported adverse events (FAERS/openFDA)#

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