Nafrinse Unit Dose Fluoride
FDA Label NDC 0273-8001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Young Dental Manufacturing Co 1, Llc. for the product Nafrinse Unit Dose Fluoride (NDC 0273-8001). 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 inactives, warning:, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Inactives

Saccharin Sodium, Potassium Sorbate, Citric Acid, Flavoring

Dye 

Warning:

For Topical use only.

Federal (USA) law prohibits  dispensing without prescription

Directions

Rinse for 1 minute and spit out. Do not swallow.

* Please review the disclaimer below.