Lucky Super Soft
FDA Label NDC 20276-550

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Delta Brands Inc for the product Lucky Super Soft (NDC 20276-550). 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, purpose, uses, warnings, stop and ask a dentist, keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Potassium nitrate - 5%

Sodium fluoride - 0.24%

Purpose

Antihypersensitivity

Anticavity

Uses

■ builds increasing protection against painful sensitivity of teeth due to cold, heat, acids, sweets or contact ■ aids in the prevention of dental cavities

Warnings

When using this product ■ if pain/sensitivity still persists after 4 weeks of use please visit your dentist

Stop And Ask A Dentist

■ if problem the persists or worsens. Sensitive teeth may indicate a serious problem that may need prompt care by a dentist.

Keep Out Of Reach Of Children

If you accidentally swallowed more than used for brushing, seek professional help or contact a Poison Control Center immediately

Directions

adults and children 12 years and older brush teeth for at least one minute, preferably after each meal, or at least twice a day, or as directed by your dentist. Be sure to brush sensitive areas

children under 12 years of age consult a dentist or doctor.

Inactive Ingredients

DC Yellow10, FDC Blue 1, flavor, glycerin, methylparaben, poly ethylene glycol 1500, propylparaben, silica, sodium benzoate, sodium carboxy methyl cellulose, sodium lauryl sulfate, sodium saccharin, sorbitol, titanium dioxide, treated water, tri sodium ortho phosphate

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