1169 Hydrogen Peroxide Spray 1364 Hydrogen Peroxide Packet

Manufacturer
Dynarex Corporation
Effective date
2025-11-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:17:00

Label at a glance#

ProductHydrogen Peroxide
Active ingredientHYDROGEN PEROXIDE
Label structure10 sections

Indications and uses

• First aid to help decrease the risk of skin infection in minor cuts, scrapes, and burns

Dosage and administration

• Clean the affected area • Apply a small amount of the product to the affected area 1 to 3 times daily • May be covered with a sterile bandage • If bandaged, let dry first • Children under 12 years of age : Consult a doctor before use

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Hydrogen Peroxide USP 3%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

• First aid to help decrease the risk of skin 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 • Over larege areas of the body • More than 1 week unless directed by a doctor

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

You have 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

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 (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Clean the affected area • Apply a small amount of the product to the affected area 1 to 3 times daily • May be covered with a sterile bandage • If bandaged, let dry first

• Children under 12 years of age: Consult a doctor before use

Other information

OTHER SAFETY INFORMATION

Store at 20º-25ºC (68º-77ºF)

Inactive ingredient

INACTIVE INGREDIENT SECTION

Purified Water

Questions?

OTC - QUESTIONS SECTION

1-888-Dynarex Monday - Friday, 9AM - 5PM EST.

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1169_IN_MASTER1169_IN_MASTER1169 Label

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1364_DM_MASTER1364_DM_MASTER1364

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130840117332775GTIN-13: 0840117332775
EAN-13: 0840117332775
GTIN-12: 840117332775
UPC-A: 840117332775
GTIN storage (14 digits): 00840117332775
1169_IN_MASTER_R240215-1.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
67777-015-05Hydrogen Peroxide1000 in 1 CASESPRAY10002
67777-015-06Hydrogen Peroxide29.6 mL in 1 PACKETSPRAY29.62
67777-015-07Hydrogen Peroxide24 in 1 CASESPRAY242
67777-015-08Hydrogen Peroxide59.1 mL in 1 BOTTLE, SPRAYSPRAY59.12

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
67777-01567777-015-08, 67777-015-07, 67777-015-06, 67777-015-05

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
Hydrogen Peroxide1169 HYDROGEN PEROXIDE SPRAYDynarex Corporation11854afb-db97-5a43-e063-6394a90aa39c2025-11-19WarningsExact identifier
ndc (package): 67777-015-06
ndc (package): 67777-015-05
ndc (package): 67777-015-08
ndc (package): 67777-015-07
ndc (product): 67777-015
ndc11 (package): 67777001505
ndc11 (package): 67777001506
ndc11 (package): 67777001508
ndc11 (package): 67777001507
spl id: 43f6590a-bb4b-7e5a-e063-6394a90af638
spl set id: 11854afb-db97-5a43-e063-6394a90aa39c

Reported adverse events (FAERS/openFDA)#

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