Vitaplus fore

Manufacturer
MY Corp.,Ltd
Effective date
2021-04-15
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:39:45

Label at a glance#

ProductVitaplus fore
Active ingredientALCOHOL, TITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Ethanol, Titanium Dioxide

INACTIVE INGREDIENT SECTION

Pinus densiflora callus extract ,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
71544-0022-12023-01-30C16284748780-1f386c649-be21-0266-e053-dadaa90a7c1abfe9c7fd-1e43-627d-e053-2a95a90ae03c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71544-0022-1Vitaplus fore4000 mL in 1 DRUMLIQUID40002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71544-0022VITAPLUS FORE (ETHANOL, TITANIUM DIOXIDE) LIQUID [MY CORP.,LTD]2Legacy NDC, 1 package rows20210417_bfe9c7fd-1e43-627d-e053-2a95a90ae03c.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71544-002271544-0022-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
c00e83d3-9980-2bfc-e053-2a95a90a7babbfe9c7fd-1e43-627d-e053-2a95a90ae03c2021-04-15WarningsExact identifier
spl id: c00e83d3-9980-2bfc-e053-2a95a90a7bab
spl set id: bfe9c7fd-1e43-627d-e053-2a95a90ae03c

Reported adverse events (FAERS/openFDA)#

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