FDA.reportPublic FDA data

Water Jel Hydrogen Peroxide

Manufacturer
Water-Jel Technologies
Effective date
2025-12-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:30:49

Label at a glance#

ProductWater Jel Hydrogen Peroxide
Active ingredientHYDROGEN PEROXIDE
Label structure9 sections

Indications and uses

first aid to help prevent infection in minor cuts, scrapes and burns

Dosage and administration

clean the affected area spray a small amount of this product on the area 1 to 3 times daily 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 Topical Solution U.S.P 3%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent 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 unless directed by a doctor

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

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

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

Other information

SPL UNCLASSIFIED SECTION

  • store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

water

Questions or comments?

OTC - QUESTIONS SECTION

855-428-6074

safeguardmedical.com

Manufactured by Water-Jel Technologies, LLC

13359 Reese Blvd. E, Huntersville, NC 28078

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

hps2.00.018hps2.00.018

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
283420hydrogen peroxide 3 % Topical SprayPSN5
283420hydrogen peroxide 30 MG/ML Topical SpraySCD5
283420hydrogen peroxide 3 % Topical SpraySY5

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
59898-403-102024-02-13C16284748780-1d6a99b39-4c4b-a426-e053-dadaa90af4c2Hydrogen Peroxide
59898-403-102022-01-28C16284748780-1d6a99b39-4c4b-a426-e053-dadaa90af4c2Hydrogen Peroxide

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59898-403-10Water Jel Hydrogen Peroxide59 mL in 1 BOTTLE, SPRAYSPRAY595

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
HYDROGEN PEROXIDEACTIVE INGREDIENTBBX060AN9V1
HYDROGEN PEROXIDEACTIVE MOIETYBBX060AN9V1
WATERINACTIVE INGREDIENT059QF0KO0R1

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
59898-40359898-403-10

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
WATER059QF0KO0RIACT
HYDROGEN PEROXIDEBBX060AN9VACTIB

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
Water Jel Hydrogen PeroxideHYDROGEN PEROXIDEWater-Jel Technologiesf508c3cb-e162-4d11-9513-ff44918f82c02025-12-31WarningsExact identifier
ndc (package): 59898-403-10
ndc (product): 59898-403
ndc11 (package): 59898040310
spl id: 474ad7d8-78f3-1c01-e063-6394a90afabb
spl set id: f508c3cb-e162-4d11-9513-ff44918f82c0

Reported adverse events (FAERS/openFDA)#

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