3% Hydrogen Peroxide Spray

Manufacturer: Universal Distribution Center LLC | Jell Pharmaceuticals Pvt Ltd.
Effective date: 2025-03-05
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 00:58:43

Label at a glance#

Product3 Hydrogen Peroxide

Active ingredientHYDROGEN PEROXIDE

Label structure7 sections

Indications and uses

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

Dosage and administration

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

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydrogen Peroxide 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 and burns

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

in the eyes or apply over large areas of the body
longer than 1 week.

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep or puncture wounds, animals bites or serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

the condition persists or gets worse
irritation, pain, or redness persists or worsens
swelling, rash, or fever develops

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Is swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

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

Other information

SPL UNCLASSIFIED SECTION

keep tightly closed and at controlled room temperature. Do not shake bottle. Hold srayer tip away from face when opening.

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
91349	hydrogen peroxide 3 % Topical Solution	PSN	1
91349	hydrogen peroxide 30 MG/ML Topical Solution	SCD	1
91349	hydrogen peroxide 3 % Topical Solution	SY	1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
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
52000-805-01	3 Hydrogen Peroxide	177 mL in 1 BOTTLE	LIQUID	177		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
52000-805	3 HYDROGEN PEROXIDE (HYDROGEN PEROXIDE) LIQUID [UNIVERSAL DISTRIBUTION CENTER LLC]	1	Current NDC, 1 package rows	20250409_2f98ba8c-0ab1-e256-e063-6394a90abe8f.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

3 Hydrogen Peroxide
HYDROGEN PEROXIDE
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
52000-805	52000-805-01

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
WATER	059QF0KO0R	IACT
HYDROGEN PEROXIDE	BBX060AN9V	ACTIB

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
3 Hydrogen Peroxide	HYDROGEN PEROXIDE	Universal Distribution Center LLC	2f98ba8c-0ab1-e256-e063-6394a90abe8f	2025-03-05	Warnings	Exact identifier ndc (package): 52000-805-01 ndc (product): 52000-805 ndc11 (package): 52000080501 spl id: 2f98bbae-95ea-1338-e063-6294a90aa1d0 spl set id: 2f98ba8c-0ab1-e256-e063-6394a90abe8f

Reported adverse events (FAERS/openFDA)#

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