Exoden Cure Powder
FDA Label NDC 70602-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Lifeon Corp. for the product Exoden Cure Powder (NDC 70602-004). 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, indications & usage, dosage & administration, warnings, otc - keep out of reach of children, inactive ingredient, 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 - Active Ingredient

Aluminum Chlorohydroxy Allantoinate 0.16%

Otc - Purpose

Oral Health Care

Indications & Usage

Provide better health to teeth and gums

Dosage & Administration


Wet your toothbrush, shake off surplus water and press into powder. Brush teeth thoroughly and rinse

Warnings

Ask a dentist before use if you have
• bleeding or redness lasting more than 2 weeks
• pain, swelling, pus, loose teeth, or more spacing between teeth
These may be signs of periodontitis, a serious form of gum disease

Otc - Keep Out Of Reach Of Children

Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away

Inactive Ingredient

Bentonite, Sodium Chloride, Xylitol, Chitosan, L-Menthol

Package Label.Principal Display Panel

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