3% HYDROGEN PEROXIDE

Manufacturer
LJ Pharma
Effective date
2025-08-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:09:24

Label at a glance#

Product3% HYDROGEN PEROXIDE
Active ingredientHYDROGEN PEROXIDE
Label structure8 sections

Indications and uses

First aid to help prevent the risk of infection in minor cuts, Scrapes & Burns. Aids in the removal of phlegm , mucus or other secretions associated with occasional sore mouth

Dosage and administration

Clean the affected Area Apply Small amount of this product on the area 1-3 times daily Let the alcohol dry on skin before using bandages. May be covered with a sterile bandag.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydrogen Peroxide (Stabilized) 3%

Purpose

OTC - PURPOSE SECTION

FIRST AID ANTISEPTIC ORAL DEBRIDING AGENT

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent the risk of infection in minor cuts, Scrapes & Burns. Aids in the removal of phlegm , mucus or other secretions associated with occasional sore mouth

Warnings

WARNINGS SECTION

  • For external use only
  • IF taken internally, Serious gastric disturbances will result.  Flammable , Keep away from fire or flame.
  • Use only in a well-ventilated area:Fumes may be toxic.

Ask a doctor before use if you havedeep or puncture wounds, Animal bites or serious burns.

When using this product:

  • Do not Apply over large areas of the body.
  • Do not use longer than one week unless directed by doctor

Stop use and ask doctor ifconditions persist or get worse

Keep out of reach of children In case of ingestion , get medical help or contact a poison. control center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean the affected Area
  • Apply Small amount of this product on the area 1-3 times daily
  • Let the alcohol dry on skin before using bandages.
  • May be covered with a sterile bandag.

Other information

SPL UNCLASSIFIED SECTION

  • Store ate room temperature
  • Do not shake bottle Hold away from face when opening.
  • Does not contain, nor is intended as a substitute for grain or ethyl alchol.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Purified Water

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
91349hydrogen peroxide 3 % Topical SolutionPSN2
91349hydrogen peroxide 30 MG/ML Topical SolutionSCD2
91349hydrogen peroxide 3 % Topical SolutionSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84809-005-013% HYDROGEN PEROXIDE236 mL in 1 BOTTLE, SPRAYLIQUID2362
84809-005-013% HYDROGEN PEROXIDE12 in 1 CARTONLIQUID122
84809-005-023% HYDROGEN PEROXIDE473 mL in 1 BOTTLE, SPRAYLIQUID4732
84809-005-023% HYDROGEN PEROXIDE12 in 1 CARTONLIQUID122
84809-005-033% HYDROGEN PEROXIDE946 mL in 1 BOTTLE, SPRAYLIQUID9462
84809-005-033% HYDROGEN PEROXIDE12 in 1 CARTONLIQUID122

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
84809-00584809-005-01, 84809-005-02, 84809-005-03

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

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
3% HYDROGEN PEROXIDEHYDROGEN PEROXIDELJ Pharmae468ad76-b26a-49f0-a2c5-a027299babc72025-08-05WarningsExact identifier
ndc (package): 84809-005-02
ndc (package): 84809-005-03
ndc (package): 84809-005-01
ndc (product): 84809-005
ndc11 (package): 84809000503
ndc11 (package): 84809000501
ndc11 (package): 84809000502
spl id: 3b9d65a2-39a5-08f0-e063-6394a90a4c91
spl set id: e468ad76-b26a-49f0-a2c5-a027299babc7

Reported adverse events (FAERS/openFDA)#

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