Otc - Active Ingredient
Active ingredient: sodium monofluorophosphate
Nbf Gingival
FDA Label NDC 23636-1001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nanocuretech for the product Nbf Gingival (NDC 23636-1001). 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
Inactive ingredient: silicon dioxide, triclosan, glycerin, d-sorbitol, polyethylene glycol, chitosan oligosaccharide, carboxymethylcellulose sodium, propolis extract, xylitol, sacccharin sodium hydroate, peppermint oil, l-menthol, sodium benzoate, ascorbic acid, tocopherol, purified water
Otc - Purpose
■ prevention of gingival disease
Otc - Keep Out Of Reach Of Children
Keep out of reach of the children
Indications & Usage
Apply toothpast on soft bristle toothbrush and brush
Warnings
If irritation occurs when using this product, discontinue use
Dosage & Administration
■ apply three times a day after meals
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