Made by Dentists Enamel 10 Fluoride Anticavity
- Product NDC
- 75065-033
- 11-digit product format
- 750650033
- Labeler code
- 75065
- Product ID
- 75065-033_5b9b278a-8dab-1f6b-e063-6394a90a788b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- POTASSIUM NITRATE, SODIUM FLUORIDE
- Dosage form
- PASTE
- Route
- DENTAL
- Labeler
- Made By Dentists Inc
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-08-01
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 50; 1.5 mg/g; mg/g
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Made by Dentists Enamel 10 Fluoride Anticavity
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| POTASSIUM NITRATE | 50 mg/g |
| SODIUM FLUORIDE | 1.5 mg/g |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|
| 75065-033-06 | 75065003306 | 1 TUBE in 1 CARTON (75065-033-06) / 120 g in 1 TUBE | 1 tube | 2026-08-01 | No | No | Current |
| 75065-033-07 | 75065003307 | 1 TUBE in 1 CARTON (75065-033-07) / 20 g in 1 TUBE | 1 tube | 2026-09-01 | Yes | No | Current |