Hydrogen Peroxide

Manufacturer: Cardinal Health, 110 dba Leader | Nice-Pak Products, LLC
Effective date: 2026-01-29
Label type: HUMAN OTC DRUG LABEL
Version: 26
Source: full-release
Hydrated at: 2026-06-01 01:36:02

Label at a glance#

ProductHydrogen Peroxide

Active ingredientHYDROGEN PEROXIDE

Label structure8 sections

Indications and uses

first aid to help prevent the risk of infection in minor cuts, scrapes and burns aids in the removal of phlegm, mucus, or other secretions associated with occasional sore mouth

Dosage and administration

First aid antiseptic: clean the affected area apply 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 Oral debriding agent (oral rinse): adults and children 2 years of age and over: mix with an equal amount of water swish around in the mouth over the affected area for at least 1 minute and then spit out use up to 4 times daily after m...

Storage and handling

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

Contacts and useful links#

PhoneLabel contact1-888-593-0593

PhoneLabel contact1-800-200-6313

Websitewww.myleader.com

www.myleader.com

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydrogen peroxide (stabilized) 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
aids in the removal of phlegm, mucus, or other secretions associated with occasional sore mouth

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

deep or puncture wounds, animal bites or serious burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

the condition persists or gets worse
sore mouth symptoms do not improve in 7 days
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

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

Directions

DOSAGE & ADMINISTRATION SECTION

First aid antiseptic:

clean the affected area
apply 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

Oral debriding agent(oral rinse): adults and children 2 years of age and over:

mix with an equal amount of water
swish around in the mouth over the affected area for at least 1 minute and then spit out
use up to 4 times daily after meals and at bedtime or as directed by a dentist or doctor

children under 12 years of age should be supervised in the use of this product
children under 2 years of age: consult a dentist or doctor

Other information

STORAGE AND HANDLING SECTION

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

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water

Questions?

OTC - QUESTIONS SECTION

1-888-593-0593

principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LEADER _™

NDC 70000-0022-1

Hydrogen Peroxide

Topical Solution USP, 3%

First Aid Antiseptic

Oral Debriding Agent

DO NOT USE IF PRINTED SEAL UNDER CAP IS BROKEN OR MISSING.

DIST. BY CAH, DUBLIN, OH 43017

www.myleader.com

1-800-200-6313

Pat. D675, 101

CIN 5516075 REV. 11/25

8 FL OZ (236 mL)

image description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
91349	hydrogen peroxide 3 % Topical Solution	PSN	26
91349	hydrogen peroxide 30 MG/ML Topical Solution	SCD	26
91349	hydrogen peroxide 3 % Topical Solution	SY	26

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Data code	Data Matrix	L0012706SC		mm01.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70000-0022-1	Hydrogen Peroxide	236 mL in 1 BOTTLE, PLASTIC	LIQUID	236		26
70000-0022-3	Hydrogen Peroxide	236 mL in 1 BOTTLE, SPRAY	LIQUID	236		26

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70000-0022-1	ML - Milliliter	70000-0022	ced34036-1f11-4584-91fb-2197901a941a	1	2020-01-03
70000-0022-3	ML - Milliliter	70000-0022	110134ec-9581-4e40-8a81-e5358c674d3e	1	2020-08-06

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
70000-0022	70000-0022-1, 70000-0022-3

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 · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
25	2026-01-21	monthly-update	2026-06-03 17:53:14

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	Cardinal Health, 110 dba Leader	d1418649-9490-4dab-b89c-9de6bb719642	2026-01-29	Warnings	Exact identifier ndc (package): 70000-0022-1 ndc (package): 70000-0022-3 ndc (product): 70000-0022 ndc11 (package): 70000002201 ndc11 (package): 70000002203 spl id: 498e94ec-e063-0431-e063-6294a90a0933 spl set id: d1418649-9490-4dab-b89c-9de6bb719642

Reported adverse events (FAERS/openFDA)#

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