Otc - Active Ingredient
sodium fluoride, allantoin
Dio Pororo Kids Foaming
FDA Label NDC 75902-3001
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 Pororo Kids Foaming (NDC 75902-3001). 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, glucosyl stevia, sodium lauroyl sarcosinate, hydroxyapatite, methylparaben, natural strawberry flavor, camellia sinensis leaf ext, water
Otc - Purpose
for dental care
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
spray out 1 time in mouth and gargle for 30 seconds
spray out 1 time in mouth and use toothbrush
Warnings
store at room temperature
Dosage & Administration
for dental use only
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