Optimax Anticavity Fluoride Watermelon Paste
NDC Package 73656-032-00
Package Information
Optimax Anticavity Fluoride Watermelon (sodium monofluorophosphate) pastes is Adults and children 2 years of age & older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. Children under 6 years of age: Instruct in good brushing and rinsing habits (to minimize swallowing). This formulation utilizes a paste delivery system. Marketed by White Glo Usa Inc, this product is identified by NDC 73656-032 and is authorized under FDA application M021.
Identification & Billing
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )Toothpaste
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 73656 - White Glo Usa Inc
- 73656-032 - Optimax Anticavity Fluoride Watermelon
- 73656-032-00 - 1 TUBE in 1 BOX / 80 g in 1 TUBE
- 73656-032 - Optimax Anticavity Fluoride Watermelon
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 73656-032-00 identifies a specific commercial package of 1 tube in 1 box / 80 g in 1 tube of Optimax Anticavity Fluoride Watermelon, a human over the counter drug labeled by White Glo Usa Inc. This paste is formulated for dental use and contains sodium monofluorophosphate as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by White Glo Usa Inc on April 04, 2025. The current certification is valid through December 31, 2026.
How is this White Glo Usa Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 73656003200. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.