Otc - Active Ingredient
colloidal silicon dioxide, tocopherol acetate, 35% hydrogen peroxide solution
Dio Whitening
FDA Label NDC 75902-4001
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 Dio Whitening (NDC 75902-4001). 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
xylityl, sorbitol solution 70%, polyethylene glycol 1500, carboxymethylcellulose sodium, xanthan gum, poly vinyl pirrolidone, sodium stannate, etc.
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 toothbrush
Warnings
store at room temperature
Dosage & Administration
for dental use only
* Please review the disclaimer below.
