Bio Spectra Gel, Dentifrice
FDA Label NDC 61649-730

10 label sections · Submitted to the FDA by 9055-7588 Quebec Inc. Dba Attitude · Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by 9055-7588 Quebec Inc. Dba Attitude for the product Bio Spectra (NDC 61649-730). 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 other, active ingredient, purpose, uses, keep out of reach of children., directions, inactive ingredient, questions?, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Other

DRUG FACTS

Active Ingredient

Sodium fluoride (0.243% w/w)

Purpose

Anti-cavity

Uses

  • Prevents, fights and protects against cavities and tooth decay.
  • Effective fluoride protection.
  • Protects teeth from acid erosion.
  • Penetrates tooth enamel to help rebuild weak spots.

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