3% Hydrogen Peroxide

Manufacturer
Streamline Polymers LLC
Effective date
2022-01-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:46:49

Label at a glance#

Product3% Hydrogen Peroxide
Active ingredientHYDROGEN PEROXIDE
Label structure13 sections

Dosage and administration

Clean the affected area apply a small amount of this product on the area 1 to 3 times daily may be covered with a sterile bandage if bandaged, let dry first.

Storage and handling

Store in a cool, dark place.

Label contents#

Full prescribing information#

Hydrogen Peroxide 3%

SPL UNCLASSIFIED SECTION

32 oz Hydrogen Peroxide32 oz Hydrogen PeroxideThis is a solution of 3% hydrogen peroxide and purified water.

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

3%Hydrogen Peroxide

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Use

INDICATIONS & USAGE SECTION

helps prevent the risk of infection in minor cuts, scrapes, burns

Warnings

WARNINGS SECTION

Do not use in the eyes or apply over large areas of the body. Do not use longer than 1 week unless directed by a doctor.

Do not use

OTC - DO NOT USE SECTION

  • in eyes or apply over large areas of the body
  • longer than 1 week unless directed by a doctor

OTC - WHEN USING SECTION

When using this product do not shake the bottle; keep away from eyes and other mucous membranes; if eye contact occurs, rinse with plenty of water.

OTC - STOP USE SECTION

Stop use and ask a doctor if condition persists or gets worse.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean the affected area
  • apply a small amount of this product on the area 1 to 3 times daily
  • may be covered with a sterile bandage
  • if bandaged, let dry first.

Other information

STORAGE AND HANDLING SECTION

  • Store in a cool, dark place.

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hydrogen Peroxide 32 oz NDC: 74793-0011-1Hydrogen Peroxide 32 oz NDC: 74793-0011-1

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74793-0011-12023-07-28C16284748780-10191ceaa-6801-198a-e063-dbdaa90aec3eHydrogen Peroxide 3%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74793-0011-13% Hydrogen Peroxide946 mL in 1 BOTTLELIQUID9462

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74793-00113% HYDROGEN PEROXIDE LIQUID [STREAMLINE POLYMERS LLC]2Legacy NDC, 1 package rows20220114_b0237838-d4b2-07d9-e053-2a95a90a35ee.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
74793-001174793-0011-1

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
HYDROGEN PEROXIDEBBX060AN9VACTIB
WATER059QF0KO0RIACT

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
d57af1b2-e36c-5d89-e053-2995a90a9987b0237838-d4b2-07d9-e053-2a95a90a35ee2022-01-13WarningsExact identifier
spl id: d57af1b2-e36c-5d89-e053-2995a90a9987
spl set id: b0237838-d4b2-07d9-e053-2a95a90a35ee

Reported adverse events (FAERS/openFDA)#

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