Cool Sense
FDA Label NDC 73706-0001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bncare Agriculture Co., Ltd. for the product Cool Sense (NDC 73706-0001). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, inactive ingredient, 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

Otc - Purpose

Can help the antimicrobial action in the mouth

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

3 times a day, spray 0.5ml (approx. 2 times) once orally

Warnings

  • Those who are allergic to propolis should be careful about their intake, and those who have a specific or allergy should check their ingredients.
  • If you experience any of the symptoms, please stop intake, consult a specialist or contact the customer service.
  • Due to the nature of the raw materials, sediment may occur occasionally, but the quality is not abnormal.
  • Check the expiration date before ingesting and follow the intake and intake method.
  • Take care that the spray nozzle does not come in direct contact with your mouth and after spraying, clean and store the spray.

Inactive Ingredient

water, gamma-cyclodextrin, xylitol, anhydrous dextrose, glucosyl steviol, citric acid monohydrate, codonopsis pilosula whole (concentrate), pear (concentrate) juice, chitosan, turmeric, artificial flavor

Dosage & Administration

For dental use only

Package Label.Principal Display Panel

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