maxim SOLUTION OF Hydrogen Peroxide

Manufacturer
Ostl, Inc.
Effective date
2016-05-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:46:05

Label at a glance#

Productmaxim Hydrogen Peroxide
Active ingredientHYDROGEN PEROXIDE
Label structure10 sections

Storage and handling

Other information Keep tightly closed and at controlled room temperature. Do not shake bottle, Hold sprayer tip away from face when opening.

Label contents#

Full prescribing information#

Active ingredients 

OTC - ACTIVE INGREDIENT SECTION

Hydrogen peroxide (stabilized) 3%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INDICATIONS & USAGE SECTION

Use first aid to help prevent the risk of infection in minor cuts, scrapes and burns 

Warnings

WARNINGS SECTION

For external use only
Do not use • in the eyes or apply over large areas of the body

                 • longer than one week

Ask a doctor before use if you have deep or puncture wounds, animal bites or serious burns.

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

DOSAGE & ADMINISTRATION SECTION

Directions • Clean the affected area • spray a small amount of product on the affected area 1 to 3 times a day • may be covered with a sterile bandage • if bandaged, let dry first

INACTIVE INGREDIENT SECTION

Inactive ingredient purified water, Phosphoric acid as a stabilizer

STORAGE AND HANDLING SECTION

Other information Keep tightly closed and at controlled room temperature.

Do not shake bottle, Hold sprayer tip away from face when opening.

SPL UNCLASSIFIED SECTION

Hydrogen Peroxide 3% Topical Solution USP

TOPICAL ANTI-INFECTIVE

For treatment of minor cuts and abrasions.

Made in India

Imported by : OSTL Inc.

5805 White Oak Ave Encino CA, 91416

WWW.OSTLTRADE.COM

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
91349hydrogen peroxide 3 % Topical SolutionPSN1
91349hydrogen peroxide 30 MG/ML Topical SolutionSCD1
91349hydrogen peroxide 3 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69950-005-022023-01-30C16284748780-1f386c649-d6ec-0266-e053-dadaa90a7c1amaxim SOLUTION OF Hydrogen Peroxide

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69950-005-02maxim Hydrogen Peroxide295 mL in 1 BOTTLE, PLASTICLIQUID2951

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69950-005MAXIM HYDROGEN PEROXIDE (HYDROGEN PEROXIDE) LIQUID [OSTL, INC.]1Legacy NDC, 1 package rows20160525_d3f63dca-3de0-4805-b8a5-407ec9311b31.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
69950-00569950-005-02

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
HYDROGEN PEROXIDEBBX060AN9VACTIB
WATER059QF0KO0RIACT
PHOSPHORIC ACIDE4GA8884NNIACT

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
cf365a61-6e9c-4ee5-af82-41eb0e218f3cd3f63dca-3de0-4805-b8a5-407ec9311b312016-05-22WarningsExact identifier
spl id: cf365a61-6e9c-4ee5-af82-41eb0e218f3c
spl set id: d3f63dca-3de0-4805-b8a5-407ec9311b31

Reported adverse events (FAERS/openFDA)#

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