Vitaplus Ore
FDA Label NDC 71544-0023

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by My Corp.,ltd for the product Vitaplus Ore (NDC 71544-0023). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Hypochlorous Acid, Titanium Dioxide

Inactive Ingredient

Orange oil,Rice bran oil,Foeniculum vulgare seed extract,Indican,Maltitol,Sorbitol,Water

Otc - Keep Out Of Reach Of Children

keep out of reach of the children

Indications & Usage

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

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.

Package Label.Principal Display Panel

1 (Label Ore)

1 (Label Ore)

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