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  5. Label Information: Dio Whitening

FDA Label for Dio Whitening

View Indications, Usage & Precautions

Table of Contents

    1. OTC - ACTIVE INGREDIENT
    2. INACTIVE INGREDIENT
    3. OTC - PURPOSE
    4. OTC - KEEP OUT OF REACH OF CHILDREN
    5. INDICATIONS & USAGE
    6. WARNINGS
    7. DOSAGE & ADMINISTRATION

Dio Whitening Product Label

The following document was submitted to the FDA by the labeler of this product Dio Corporation. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Otc - Active Ingredient



colloidal silicon dioxide, tocopherol acetate, 35% hydrogen peroxide solution



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


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