Dentalux sensitive
- Product NDC
- 71141-169
- Requested package NDC
- 71141-169-32
- 11-digit product format
- 711410169
- Labeler code
- 71141
- Product ID
- 71141-169_d9a0653d-f3f7-8d4c-e053-2a95a90abfe8
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Potassium nitrate, sodium fluoride
- Dosage form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Labeler
- Lidl US LLC
- Application
- part356
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2021-05-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM NITRATE; SODIUM FLUORIDE
- Active strength
- 5 g/100g; g/100g
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71141-169-32 | 71141016932 | 159 g in 1 TUBE (71141-169-32) | 159 g | 2021-05-01 | 0000-00-00 | No | No | Current |