Hydrogen Peroxide Spray

Manufacturer: HART Health | Safetec of America, Inc
Effective date: 2024-01-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:07:47

Label at a glance#

ProductHydrogen Peroxide

Active ingredienthydrogen peroxide

Label structure8 sections

Indications and uses

First aid to help prevent skin infection in minor cuts and scrapes

Dosage and administration

Adults and children 12 years of age and over: clean the affected area spray a small amount of this product on the area 1 to3 times daily when dry, may be covered with a sterile bandage Childred under 12 year of age: ask a doctor

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydrogen Peroxide 3.0%

Purpose

OTC - PURPOSE SECTION

Topical Antiseptic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent skin infection in minor cuts and scrapes

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

in or near the eyes
over large portions of the body
on animal bites
on deep or puncture wounds
on raw surfaces
on blistered areas
on serious burns
for more than 7 days unless directed by a doctor

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or lasts more than 7 days
symptoms clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medicla help or contact a Poison Control Center right away. 1-800-222-1222

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over:

clean the affected area
spray a small amount of this product on the area 1 to3 times daily
when dry, may be covered with a sterile bandage

Childred under 12 year of age: ask a doctor

Other information

OTHER SAFETY INFORMATION

sotre at 68° to 77°F (20° to 25°C)

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2748hydrogenv19f.jpg

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
283420	hydrogen peroxide 3 % Topical Spray	PSN	1
283420	hydrogen peroxide 30 MG/ML Topical Spray	SCD	1
283420	hydrogen peroxide 3 % Topical Spray	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
3c386306-c48a-413e-bb69-70cb268496f3	Product name	1	20210727
5eb9f24b-9328-475e-af0a-18021935eb6a	Product name	1	20180220

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
50332-0219-2	Hydrogen Peroxide	60 mL in 1 BOTTLE, SPRAY	SPRAY	60		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
50332-0219	HYDROGEN PEROXIDE SPRAY [HART HEALTH]	1	Current NDC, 1 package rows	20240125_0346a322-8f6e-405a-8d17-8bc6ce5105a3.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 2 matching rows.

Hydrogen Peroxide
water

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
50332-0219	50332-0219-2

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
Name	UNII	Kind
hydrogen peroxide	BBX060AN9V	ACTIB
water	059QF0KO0R	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Hydrogen Peroxide	HYDROGEN PEROXIDE	HART Health	0346a322-8f6e-405a-8d17-8bc6ce5105a3	2024-01-24	Warnings	Exact identifier ndc (package): 50332-0219-2 ndc (product): 50332-0219 ndc11 (package): 50332021902 spl id: 49eed8c5-8b5e-442f-8354-04c4403484e5 spl set id: 0346a322-8f6e-405a-8d17-8bc6ce5105a3

Reported adverse events (FAERS/openFDA)#

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