Inactive Ingredient
Aqua, Xylitol, Aloe, Glycerin, Menthol, Sodium Benzoate, Citric acid
Cureforte Breath Reset Spray
FDA Label NDC 85884-025
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Steel City Health Private Limited for the product Cureforte Breath Reset (NDC 85884-025). 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 inactive ingredient, indications & usage, warnings, otc - purpose, otc - keep out of reach of children, dosage & administration, 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
Indications & Usage
Usage:
For temporary relief of dry mouth
Helps kill germs that cause bad breath
Helps reduce plaque that leads to early gum problems
Freshens breath
Warnings
Warnings:
For oral use only.Do not swallow. Not for children under 6 years of age Stop use and
ask a doctor if irritation or discomfort occurs. Keep out of reach of children
Otc - Purpose
Purpose:
Glycerin – Temporarily relieves dry mouth
-Cetylpyridinium Chloride – Helps reduce germs that cause bad breath and plaque
Otc - Keep Out Of Reach Of Children
Warnings: For oral use only.Do not swallow. Not for children under 6 years of age Stop use and
ask a doctor if irritation or discomfort occurs. Keep out of reach of children
* Please review the disclaimer below.
