Otc - Active Ingredient
sodium fluoride
Pure Mouth Liquid
FDA Label NDC 72875-0001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by On On Co., Ltd. for the product Pure Mouth Liquid (NDC 72875-0001). 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, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Sodium fluoride
Sodium saccharin
DL-Alanine
Citric acid
Sodium citrate
Xylitol
Green extract
Licorice extract
Mugwort extract
Ginger Tincture
Sodium benzoate
l-menthol
Spearmint flavor
Purified water
Otc - Purpose
Remove bad breath, prevent tooth decay
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Use twice a day (morning and evening), use 10-15ml for one time,
take your mouth for about 30 seconds Rinse and spit out
Warnings
Keep the prescribed usage, capacity.
When using in children, please use under the guidance and supervision of the guardian.
Use only for mouthwash, do not use for internal use, guitar)
Do not use for children under 6 years old unless directed by a pharmacist or doctor.
Dosage & Administration
for oral use only
Package Label.Principal Display Panel
Label (Label)
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