Active Ingredient
Active ingredients: Sodium Monofluorophosphate 0.01%
An Tooth
FDA Label NDC 69153-120
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by An Co Ltd. for the product An Tooth (NDC 69153-120). 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, warnings, keep out of reach of children, directions, 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
Inactive ingredients: Precipitated Calcium Carbonate, D-Sorbitol Solution, Glycerin, Sodium Lauryl Sulfate, Polyethylene Glycol 1500, Carboxymethylcellulose Sodium, Mentha Oil, l-Menthol, Methyl ρ-Hydroxybenzoate, Steviol Glycoside, Aminocaproic Acid, Xylitol, Aluminum Chlorohydroxy Allantoinate, Dibasic Calcium Phosphate Hydrat, Chitosan, Propolis Extract, Argentum, FD&C Blue No.1, Deionized Water
Purpose
Purpose: Anticaries
Warnings
Warnings: 1. Try not to swallow toothpaste, gargle enough with water. 2. If a problem arises as these toothpaste, consult to dentist or physician after stop the using. 3. If use a children under six years of age, just use like pea-sized amount and supervise child’s brushing and rinsing. 4. If swallowed the toothpaste a children under six years of age, immediately consult with dentist or physician. 5. Keep this product out of the reach of children under six years of age.
Keep Out Of Reach Of Children
Keep this product out of the reach of children under six years of age.
Directions
Directions: Brush teeth with balance of toothpaste.
Directions: Brush teeth with balance of toothpaste.
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