Active Ingredient
Sodium Bicarbonate
Natural Tooth Powder
FDA Label NDC 84732-049
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dongguan Haiyi Technology Co.,ltd. for the product Natural Tooth Powder (NDC 84732-049). 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 active ingredient, inactive ingredient, purpose section, warning, stop use, not use, out of children, how to use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Hydroxyapatite,Calcium Carbonate, Kaol,Mentha Piperita (Peppermint) Oil, Cocos Nucifera (Coconut) Oil,Pearl Powder,
Purpose Section
Natural, fluoride-free, and does not contain hydrogen peroxide.
Warning
Choosingthe right tooth powder is very important for oral health.In addition, when using tooth powder, you should avoid swallowing too much powder to avoid discomfort. lf you have special dental ororal conditions, it is recommended to seek advice from your dentistor dental specialist.
Stop Use
This product may cause allergic reactions in asmall number of people.
lf you experience any discomfort,please stop using it immediately.
Not Use
Not suitable for use by children, pregnantor breast feeding people.
Out Of Children
KEEP THE PRODUCT OUT OF REACH OF CHILDREN to
How To Use
After moistening the toothbrush, gently apply an appropriate amountof tooth powder.Brush your teeth gently with a toothbrush containing tooth powder,trying to cover all tooth surfaces.Rinse your mouth thoroughly with water until there is no remainingtooth powder in your mouth.
Dosage
Once a day in the morning and evening
Package Label.Principal Display Panel
Label (Fdc22d913385478ca406158668d806cc)
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