Vitaplus eco hygiene

Manufacturer
MY Corp.,Ltd
Effective date
2021-05-10
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:40:17

Label at a glance#

ProductVitaplus eco hygiene
Active ingredientHYPOCHLOROUS ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

hypochlorous acid

INACTIVE INGREDIENT SECTION

Foeniculum vulgare seed extract, Indican, Maltitol, Sorbitol, Water

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Do not dilute.• Use at strength for maximum effectiveness.• For equipment or products that are difficult to spray, apply liquid to clean gauze or cotton swab.

WARNINGS SECTION

Warnings

For external use only.

When using this product • Keep out of eyes • In case of contact with eyes, flush thoroughly with water.

Stop use and ask a doctor ifirritation or redness develop and persist for more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71544-0024-12023-01-30C16284748780-1f386c64a-392b-0266-e053-dadaa90a7c1abfd4d3fa-7b25-5286-e053-2995a90a279e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71544-0024-1Vitaplus eco hygiene4000 mL in 1 DRUMLIQUID40004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71544-0024VITAPLUS ECO HYGIENE (HYPOCHLOROUS ACID) LIQUID [MY CORP.,LTD]4Legacy NDC, 1 package rows20210511_bfd4d3fa-7b25-5286-e053-2995a90a279e.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71544-002471544-0024-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
c1f4bcc0-9372-fa26-e053-2995a90a794abfd4d3fa-7b25-5286-e053-2995a90a279e2021-05-10WarningsExact identifier
spl id: c1f4bcc0-9372-fa26-e053-2995a90a794a
spl set id: bfd4d3fa-7b25-5286-e053-2995a90a279e

Reported adverse events (FAERS/openFDA)#

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