HEB 871.001/871AA

Manufacturer
H E B | Nice-Pak Products, LLC
Effective date
2026-09-28
Label type
HUMAN OTC DRUG LABEL
Version
15
Source
daily-update
Hydrated at
2026-09-30 01:02:24

Label at a glance#

ProductHydrogen Peroxide
Active ingredientHYDROGEN PEROXIDE
Label structure14 sections

Dosage and administration

clean the affected area spray a small amount of the 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 (stabilized) 3%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic

Use

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 pucture 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 the 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

OTHER SAFETY INFORMATION

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

Adverse Reaction

ADVERSE REACTIONS SECTION

MADE WITH PRIDE & CARE FOR H-E-B  ®

SAN ANTONIO, TX 78204

100% GUARANTEE promise

Principal display panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

H-E-B  ®

Hydrogen Peroxide

Topical Solution USP

First Aid Antiseptic

  • For Treatment of Minor Cuts and Abrasions

10 FL OZ (295 mL)

image descriptionimage descriptionimage descriptionimage description

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 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
37808-87137808-871-43, 37808-871-45, 37808-871-72

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 · Source PDF

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
142026-02-24full-release2026-06-01 01:47:19

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
4b9436b4-e31f-e00b-e063-6294a90a721ede0e099b-3516-4040-85a1-cc101df75a322026-02-24WarningsExact identifier
spl set id: de0e099b-3516-4040-85a1-cc101df75a32

Reported adverse events (FAERS/openFDA)#

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