Otc - Active Ingredient
Active ingredient
Sodium Monofluorophosphate 0.758% (0.1% w/v fluoride ion)
Dr. Noah Kids Tooth Paste, Dentifrice
FDA Label NDC 82989-040
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Project Noah Inc. for the product Dr. Noah Kids Tooth (NDC 82989-040). 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, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, other safety information, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Anti-cavity
Indications & Usage
Use
■ Aids in the prevention of dental cavities.
Warnings
Warnings
■ Keep out of reach of children under 6 years of age.
■ If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Otc - Keep Out Of Reach Of Children
■ Keep out of reach of children under 6 years of age.
Dosage & Administration
Directions
■ Children under 2 years: Consult a dentist or doctor.
■ Children 2–6 years: Use pea-sized amount. Supervise child.
■ Adults and children 6+: Brush twice daily. Do not swallow.
Other Safety Information
Other Information
■ Airtight container, Store at room temperature (1~30°C)
Otc - Questions
Questions
■ https://drnoah.us/
Inactive Ingredient
Inactive ingredients
Silicon Dioxide, D-Sorbitol Solution, Concentrated Glycerin, Carboxymethylcellulose Sodium, Sodium Bicarbonate, Hydroxyapatite, Xylitol, Enzymatically Modified Stevia, Lemon Oil, Natural Citron Flavor, Natural Raspberry Flavor, Sodium Cocoyl Glutamate, Water
* Please review the disclaimer below.
