Active Ingredients
Sodium Fluoride 0.243%
Oral Fusion Anticavity
FDA Label NDC 70766-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yangzhou Sion Commodity Co.,ltd for the product Oral Fusion Anticavity (NDC 70766-010). 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, warnings, otc - keep out of reach of children, directions, inactive ingredient, 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
Purpose
anticavity
Uses
Help protect against cavities
Warnings
Keep out of the reach of children under 6 years of age. If more than used for brushing is accidently swallowed,get medical help or contact a Poison Control Center immediately.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
Adult and children 2 years of age and older:
- Brush teeth thoroughly after meal or at least twice a day, or use as directed by a dentist.
- Do not swallow
- To minimizing swallowing, use only a pea sized amount in children under 6
- and supervise children's brushing and rinsing to minimize swallowing.
- Ask a dentist
Under 2 years:
Inactive Ingredient
Sorbitol, Water, Hydrated Silica, Disodium pyrophosphate, Flavor, Sodium Hydroxide, Xanthan Gum, Cellulose Gum, Hydroxypropyl Guar, Methyl Paraben Sodium, Propyl Paraben Sodium, Sodium Saccharin, Water, Sodium Lauryl Sulfate, CI 778891
Package Label.Principal Display Panel
Image Description (Label)
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