Mediaqua premium

Manufacturer
Mediecotech co ltd
Effective date
2020-09-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:26:42

Label at a glance#

ProductMediaqua premium
Active ingredientHYPOCHLOROUS ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Hypochlorous Acid

INACTIVE INGREDIENT SECTION

WATER, sodium chloride

OTC - PURPOSE SECTION

sterilization, disinfection

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Apply an appropriate amount on your hands and rub well to dry.

WARNINGS SECTION

1. Do not use on the following body parts. A wide range of body parts and damaged skin around the eyes and ears, in the oral cavity (may have irritating effects)
2. If the following symptoms appear, stop using them immediately and consult a doctor or pharmacist.
1) Hypersensitivity symptoms such as rash, erythema, itching, and edema
2) Skin irritation symptoms

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1604557hypochlorous acid 0.01 % Topical SolutionPSN1
1604557hypochlorous acid 0.1 MG/ML Topical SolutionSCD1
1604557hypochlorous acid 0.01 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80458-0001-12022-01-28C16284748780-1d6a99b39-e0e9-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80458-0001-1Mediaqua premium500 mL in 1 BOTTLELIQUID5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80458-0001MEDIAQUA PREMIUM (HYPOCHLOROUS ACID) LIQUID [MEDIECOTECH CO LTD]1Legacy NDC, 1 package rows20200903_ae5b7358-19cd-417f-e053-2995a90a54a2.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
80458-000180458-0001-1

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
WATER059QF0KO0RIACT
HYPOCHLOROUS ACID712K4CDC10ACTIB
SODIUM CHLORIDE451W47IQ8XIACT

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
ae5b7cf2-c262-8f1f-e053-2a95a90aa171ae5b7358-19cd-417f-e053-2995a90a54a22020-09-02WarningsExact identifier
spl id: ae5b7cf2-c262-8f1f-e053-2a95a90aa171
spl set id: ae5b7358-19cd-417f-e053-2995a90a54a2

Reported adverse events (FAERS/openFDA)#

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