PHARMACYS PRESCRIPTION HYDROGEN PEROXIDE

Manufacturer
Ningbo Liyuan Daily Chemical Products Co.,Ltd. | Ningbo Liyuan Daily Chemical Products Co., Ltd.
Effective date
2018-08-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:47:56

Label at a glance#

ProductPHARMACYS PRESCRIPTION HYDROGEN PEROXIDE
Active ingredientHYDROGEN PEROXIDE
Label structure13 sections

Indications and uses

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

Dosage and administration

first aid antiseptic: clean affected area apply small amount of product on affected area 1-3 times a day may be covered with a sterile bandage if bandage, 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 affected area for at least 1 minute and then spit out use up to 4 times daily after meals and at bedtim...

Storage and handling

Keep tightly closed and in a dark place at a controlled room temperature. Do not shake bottle. Hold away from face when opening.

Label contents#

Full prescribing information#

Active ingredient (by volume)

OTC - ACTIVE INGREDIENT SECTION

Hydrogen peroxide 3%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic/oral debriding agent

Uses

INDICATIONS & USAGE SECTION

  • first aid to help prevent the risk of infection in minor cuts, scapes 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 the eyes or apply over large areas of the body
  • longer than one week
  • on deep or puncture wounds, animal bites, or on serious burns.

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 within 7 days
  • irritation, pain or redness persists or worsens
  • swelling, rash or fever develops

Keep this and all drugs out of the reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek professional or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

first aid antiseptic:

  • clean affected area
  • apply small amount of product on affected area 1-3 times a day
  • may be covered with a sterile bandage
  • if bandage, 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 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

OTHER SAFETY INFORMATION

  • children under 12 years 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 in a dark place at a controlled room temperature.

Do not shake bottle. Hold away from face when opening.

Inactive ingredient

INACTIVE INGREDIENT SECTION

purified water, also contains 0.001 percentage Phosphoric acid as a stabilizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
76176-11176176-111-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROGEN PEROXIDEBBX060AN9VACTIB
WATER059QF0KO0RIACT
PHOSPHORIC ACIDE4GA8884NNIACT

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
7982c043-29fb-1018-e053-2991aa0ab41c7982c043-29fa-1018-e053-2991aa0ab41c2018-08-31WarningsExact identifier
spl id: 7982c043-29fb-1018-e053-2991aa0ab41c
spl set id: 7982c043-29fa-1018-e053-2991aa0ab41c

Reported adverse events (FAERS/openFDA)#

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