Optimax Professional Whitening Anticavity Fluoride
- Product NDC
- 73656-036
- 11-digit product format
- 736560036
- Labeler code
- 73656
- Product ID
- 73656-036_3f1861dc-cfda-39f6-e063-6294a90ac367
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- SODIUM MONOFLUOROPHOSPHATE
- Dosage form
- KIT
- Labeler
- WHITE GLO USA INC
- Application
- M021
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-12-08
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Optimax Professional Whitening Anticavity Fluoride
- Listing expiration
- 2026-12-31
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Rxcui | 545626 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73656-036-00 | Optimax Professional Whitening Anticavity Fluoride | 1 in 1 KIT | KIT | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 73656-036-00 | 73656003600 | 1 KIT in 1 KIT (73656-036-00) * 1 TUBE in 1 BOX (73656-037-00) / 150 g in 1 TUBE | 1 kit | 2025-12-08 | No | No | Current |