Farmasi Whitening Paste, Dentifrice
FDA Label NDC 74690-012

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Farmasi Us Llc for the product Farmasi Whitening (NDC 74690-012). 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 ingredients, purpose, uses, keep out of reach of children, directions, inactive ingredients, questions or comments?, package labeling:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Sodium Fluoride 0.24 %
(0.15% w/v fluoride ion)

Purpose

Anticavity

Uses

Helps proctect teeth and prevents cavities. Whitens teeth by removing surface stains.

Keep Out Of Reach Of Children

under 6 years of age. If more than used for brushing in accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 6 years of age and older: brush teeth thoroughly after meals of at least twice a day, or as directed by a dentist or physician.

Inactive Ingredients

Calcium Carbonate, Sorbitol, Water/Aqua, Hydrated Silica, Lauryl Glucoside, Xanthan Gum, Flavour/Aroma, Titanium Dioxide, Sodium Benzoate, Sodium Saccharin, Tea Tree Oil/Melaleuca Alternifolia Leaf Oil, Panax Ginseng Root Extract, Aloe Juice/Aloe Barbadensis Leaf Juice, Salvadora Persica Bark/Root Extract.

Questions Or Comments?

[email protected] 1 786 238 7338 Monday - Friday (9 a.m - 6 p.m.EST)

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