PHARMACYS PRESCRIPTION HYDROGEN PEROXIDE

Manufacturer
American Consumer Products Corp
Effective date
2018-08-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:56:42

Label at a glance#

ProductPHARMACYS PRESCRIPTION HYDROGEN PEROXIDE
Active ingredientHYDROGEN PEROXIDE
Label structure9 sections

Dosage and administration

Directions 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 me...

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (by volume)

Hydrogen peroxide 3%

Purpose

OTC - PURPOSE SECTION

First aid antiseptic/oral debriding agent.

Warnings

WARNINGS SECTION

Warnings

For external use only.

Stop Use

OTC - STOP USE SECTION

Stop use and ask a doctor if: 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 out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all drugs out of the reach of children. If swallowed, seek professional or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions

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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredient

Purified water, also contains 0.001% Phosphoric acid as a stabilizer.

Indications & Usage Section

Do not use

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hydrogen Peroxide 01Hydrogen Peroxide 01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
91349hydrogen peroxide 3 % Topical SolutionPSN1
91349hydrogen peroxide 30 MG/ML Topical SolutionSCD1
91349hydrogen peroxide 3 % Topical SolutionSY1

DailyMed Product Concepts#

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
72197-008-162020-01-31C16284748780-19d75b9d0-8ee7-f424-e053-dadaa90a57cePharmacy's Prescription 16OZ Hydrogen Peroxide

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72197-008-16PHARMACYS PRESCRIPTION HYDROGEN PEROXIDE473 mL in 1 BOTTLE, PLASTICLIQUID4731

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72197-008PHARMACYS PRESCRIPTION HYDROGEN PEROXIDE (HYDROGEN PEROXIDE) LIQUID [AMERICAN CONSUMER PRODUCTS CORP]1Legacy NDC, 1 package rows20180831_72dcacd3-ddc6-a224-e053-2991aa0aa603.zip

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
72197-00872197-008-16

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
72dcacd3-ddc7-a224-e053-2991aa0aa60372dcacd3-ddc6-a224-e053-2991aa0aa6032018-08-07WarningsExact identifier
spl id: 72dcacd3-ddc7-a224-e053-2991aa0aa603
spl set id: 72dcacd3-ddc6-a224-e053-2991aa0aa603

Reported adverse events (FAERS/openFDA)#

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