Otc - Active Ingredient
sodium fluoride
Dental Pro
FDA Label NDC 41525-6001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Pbs Co., Ltd. for the product Dental Pro (NDC 41525-6001). 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
purified water, ethyl alcohol, allantoin, glycerin, xylitol, sodium saccharin, green tea, malic acid, lactic acid, sodium benzoate, citric acid peg-40 hydrogenated castor oil, sodium citrate, l-menthol, red ginseng ext, ulmus ext, red ginseng fragrance, mint fragrance, houttuynia ext, propolis ext, caramel color
Otc - Purpose
for dental care
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
① Turn the container cap and open, pour The Gargle into the cap about 10-15ml (not to overflow the cap) and
put into mouth.
② Goggle it thoroughly all over the inner mouth about 10 seconds.
③ After ②, in order to sterilize mouth, hold the liquid in the mouth about 30 seconds and spit out
Warnings
do not swallow
Dosage & Administration
for oral administration
* Please review the disclaimer below.
