Optimax Anticavity Fluoride Watermelon
- Product NDC
- 73656-032
- 11-digit product format
- 736560032
- Labeler code
- 73656
- Product ID
- 73656-032_34f34256-f481-6fe6-e063-6394a90af80b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM MONOFLUOROPHOSPHATE
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- WHITE GLO USA INC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-04-04
- Substance
- SODIUM MONOFLUOROPHOSPHATE
- Active strength
- 7.6 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Optimax Anticavity Fluoride Watermelon
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SODIUM MONOFLUOROPHOSPHATE | 7.6 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | C810JCZ56Q |
| Rxcui | 545626 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73656-032-00 | Optimax Anticavity Fluoride Watermelon | 1 in 1 BOX | PASTE | 1 | | 1 |
| 73656-032-00 | Optimax Anticavity Fluoride Watermelon | 80 g in 1 TUBE | PASTE | 80 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73656-032 | OPTIMAX ANTICAVITY FLUORIDE WATERMELON (SODIUM MONOFLUOROPHOSPHATE) PASTE [WHITE GLO USA INC] | 1 | Current NDC, 2 package rows | 20250514_b506df13-649f-4615-bc25-6ae08bd56b18.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73656-032-00 | 73656003200 | 1 TUBE in 1 BOX (73656-032-00) / 80 g in 1 TUBE | 1 tube | 2025-04-04 | No | No | Historical |