Otc - Active Ingredient
active ingredient: xylitol
Tooth Whole White
FDA Label NDC 60319-5001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hankuk Bowonbio Co., Ltd for the product Tooth Whole White (NDC 60319-5001). 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
cetylpyridinium chloride, lactose monohydrate, corn starch, d-sorbitol, ubidecarenone, glycyrrhizae extract, tea chatechin, hydroxyapatite, propolis extract, menthol powder, spirulina color
Otc - Purpose
whiten and strong teeth
removal of bad breath
prevention of gingivitis and periodontitis
prevention of periodontal diseases and gum diseases
removal of dental plaque
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
apply Proper Amount of the toothpaste on the tooth.
Warnings
Dosage & Administration
brush your teeth by putting appropriate amount of powder
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