Dentalux Anti-cavity Fluoride Paste, Dentifrice
FDA Label NDC 71141-186
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lidl Us, Llc for the product Dentalux Anti-cavity Fluoride (NDC 71141-186). 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 drug facts, active ingredient, purpose, uses, otc - keep out of reach of children, directions, inactive ingredients, questions or comments?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Sodium Monofluorophosphate 0.76%
(0.13% w/v Fluoride ion)
Purpose
Anticavity
Uses
helps protect against cavities.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.
Directions
• adults and children 2 years and older: brush teeth thoroughly after meals or at least twice a day or use as directed by a dentist.
• do not swallow.
• children 2 to 6 years: to minimize swallowing use a pea-sized amount and supervise children's brushing and rinsing until good habits are established.
• children under 2 years of age: Consult a dentist or doctor.
Inactive Ingredients
Sorbitol, Hydrated Silica, Treated Water (Aqua), Poly Ethylene Glycol 1500 (PEG 32), Sodium Lauryl Sulphate, Glycerin, Flavor, Cellulose Gum, Titanium Dioxide (CI 77891), Tetra Sodium Pyrophosphate, Sodium Benzoate, Benzyl Alcohol, Sodium Saccharin, Trisodium Phosphate
Questions Or Comments?
Call toll free 1-877-274-8358
Packaging
Dentalux Anti-cavity (7114118610)
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