Sensitive Extra Whitening
- Product NDC
- 64024-506
- 11-digit product format
- 640240506
- Labeler code
- 64024
- Product ID
- 64024-506_5b9af61a-69ea-f65c-e063-6394a90a03c4
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fluoride
- Dosage form
- PASTE
- Route
- ORAL
- Labeler
- ALDI INC.
- Application
- M022
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2026-09-15
- Substance
- SODIUM FLUORIDE; POTASSIUM NITRATE
- Active strength
- .15; 5 g/100g; g/100g
- 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
- Sensitive Extra Whitening
- Listing expiration
- 2027-12-31
Active Ingredients#
| Ingredient | Strength |
|---|---|
| SODIUM FLUORIDE | .15 g/100g |
| POTASSIUM NITRATE | 5 g/100g |
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 |
|---|---|---|---|---|---|---|---|
| 64024-506-18 | 64024050618 | 1 TUBE in 1 CARTON (64024-506-18) / 113 g in 1 TUBE | 1 tube | 2026-09-15 | No | No | Current |