Otc - Active Ingredient
Active ingredients: sodium fluoride, allantoin
Whitening Foaming-toothpaste
FDA Label NDC 75902-2001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dio Corporation for the product Whitening Foaming-toothpaste (NDC 75902-2001). 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, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Inactive ingredients: ethanol sodium lauryl sulfact, xylitol, sodium saccharin, ginger, mugwort extract, cnidium extract, mint, methylparaben, water
Otc - Purpose
For dental care
Otc - Keep Out Of Reach Of Children
Keep out of reach of the children
Indications & Usage
Brush teeth with your tooth brush or gargle after spraying it into your mouth
Warnings
Store at room temperature
Dosage & Administration
Use when neededdental use only
* Please review the disclaimer below.
